Seeds

ABSTRACT

This invention relates to a method for modifying cell proliferation in a plant which comprises the step of transforming a plant, or plant propagating material, with a nucleic acid molecule comprising at least one regulatory sequence capable of directing expression within the integuments and/or seed coat and at least one nucleic acid sequence whose expression or transcription product is capable of directly or indirectly modulating cell proliferation, whereby on expression of that nucleic acid sequence cell proliferation is modified. The invention also relates to a plant which includes a nucleic acid molecule comprising at least one regulatory sequence capable of directing expression within integuments and/or seed coat an at least one nucleic acid sequence whose expression or transcription product is capable of directly or indirectly modulated cell proliferation, whereby on expression of that nucleic acid sequence cell proliferation is modified. The invention also relates to reproducible plant material including a nucleic acid molecule comprising at least one regulatory sequence capable of directing expression within integuments and/or seed coat and at least one nucleic acid sequence whose expression or transcription product is capable of directly or indirectly modulated cell proliferation, whereby expression of that nucleic acid sequence cell proliferation is modified. According to another aspect of the invention, there is provided a method for modifying cell proliferation in a plant which comprises the step of modulating the response of the plant to an auxin in which cell proliferation is modified to produce larger or smaller seeds than wild-type.

FIELD OF THE INVENTION

The present invention relates particularly, though not exclusively, tomethods for modifying characteristics such as seed size in plants,especially flowering plants, and to plants and reproducible plantmaterial produced by the methods. The invention also relates to nucleicacid constructs for use in such methods, as well as to modified plantsand reproducible plant material per se.

BACKGROUND OF THE INVENTION

The seeds industry can be split into two high-value, commercial sectors:seeds for field crops such as corn, oil seeds, sugar beet and cereals,and vegetable and flower seed. The scientific improvement of crop plantshas gone through a succession of innovations leading to the developmentof hybrid varieties for many crops and, most recently, to theintroduction of genetically enhanced crops. The worldwide commercialseeds market is valued at around $30 billion (International SeedFederation).

1. Importance of Seed Size

Yield in crop plants where seed is the harvested product is usuallydefined as weight of seed harvested per unit area (Duvick, 1992).Consequently, individual seed weight is regarded as a major determinantof yield. Increasing seed size is desirable because it may increasetotal yield (Reynolds et al., 2001). There is also evidence that seedsize (weight) is positively correlated with a number of components of‘seed quality’ such as the percentage of germination (Schaal, 1980;Alexander and Wulff, 1985; Guberac et al, 1998); time to emergence(Winn, 1985; Wulff, 1986); durability (survival under adverse growingconditions) (Krannitz et al, 1991; Manga and Yadav, 1995); and growthrate (Marshall, 1986). Seed quality is an important factor in the costof production of commercial seed lots since these must be tested beforesale. Consequently, increasing total seed weight, even without increasesin total seed yield, may have economic benefits through improvements inseed quality. Conversely, decreasing seed size may also be desirable insome circumstances, for example by facilitating water uptake requiredfor germination (Harper et al., 1970), or in plants grown for theirfruit.

Modification of seed size is also likely to improve yield throughincreasing the ‘sink strength’ of the seed (i.e. its capacity to demandnutrients from the seed parent), or increasing the period in which theseed is acting as a strong sink. It is well established that the demandsof sink organs such as seeds have significant control over the rate ofphotosynthesis and the movement of photoassimilates from source to sinktissues (Patrick and Offler, 1995; Paul and Foyer, 2001). In wheat, theseed parent can supply more nutrients than developing seeds are able todemand for the first 15-20 days after pollination (Austin, 1980).Therefore modifications that enable seeds to draw nutrients earlier indevelopment, for example by speeding up seed growth, will allow seeds tocapture resources that would otherwise be wasted. An ‘improvedsource-sink balance permitting higher sink demand during grainfilling’has also been proposed as a method for increasing yield in wheat(Reynolds et al., 2001).

2. Composition of Seeds

Mature seeds of flowering plants consist of three components: the seedcoat, which is of exclusively maternal origin; and the two fertilizationproducts, embryo and endosperm, which have maternal and paternal geneticcontributions. Seeds develop from fertilized ovules. Ovule developmenthas been described for many species (Bouman, 1984), includingArabidopsis thaliana (Robinson-Beers et al., 1992; Schneitz et al.,1995). The main structures of the mature ovule are: the embryo sac,which contains the female reproductive cells (egg and central cell); thenucellus, which surrounds the embryo sac at least partially; and theinner and outer integuments, which envelop the embryo sac and nucellus.After fertilization the embryo and nutritive endosperm develop insidethe embryo sac while the integuments differentiate into the seed coat,which expands to accommodate the growing endosperm and embryo.

Most monocotyledonous plants, e.g. cereals including maize, wheat, rice,and barley (see Esau, 1965), produce albuminous seeds—that is, atmaturity they contain a small embryo and a relatively massive endosperm.Most dicotyledonous plants, e.g. Brassica napus, (oil seed rape,canola), soybean, peanut, Phaseolus vulgaris (e.g. kidney bean, whitebean, black bean) Vicia faba (broad bean), Pisum sativum (green pea),Cicer aeietinum (chick pea), and Lens culinaris (lentil), produceexalbuminous seeds—that is, the mature seeds lack an endosperm. In suchseeds the embryo is large and generally fills most of the volume of theseed, and accounts for almost the entire weight of the seed. Inexalbuminous seeds the endosperm is ephemeral in nature and reachesmaturity when the embryo is small and highly immature (usuallyheart/torpedo stage). Commonly embryo development depends on thepresence of the endosperm, which is generally accepted to act as asource of nutrition for the embryo.

3. Control of Seed Size

Seed size control can be viewed from the perspective of (1)‘development’—the extent of cell division and expansion in one or moreseed components (e.g. Reddy and Daynard, 1983; Swank et al, 1987; Scottet al., 1998; Garcia et al., 2003) or (2) ‘metabolism’13 metabolicactivity and transport of nutrients within the seed and between the seedand seed parent (e.g. Weber et al., 1996, 1997). Development andmetabolism are interdependent: for example, invertase activity (involvedin hexose transport) at the boundary of maternal tissues and endospermor embryo sac is required for endosperm proliferation in maize (Cheng etal., 1996), and high invertase activity is correlated with increasedcell numbers in broad bean seed coat (Weber et al., 1996), legumeembryos (Weber et al., 1997), and barley endosperm (Weschke et al.,2003). Our present investigations focus on the developmental aspects ofseed size control, although it can be assumed that changes to celldivision/expansion in the seed will also be correlated with changes inmetabolic activity and nutrient flow.

3a. Endosperm-Led Seed Growth

Several studies show a correlation between endosperm growth and finalseed size, for example in maize (Lin, 1984; Jones et al., 1996), andeven in the dicot Arabidopsis thaliana, which has an ephemeral endosperm(Scoff et al., 1998; Garcia et al., 2003). Work in our laboratory hasshown that overproliferation of the endosperm leads to large seeds withlarge embryos, while inhibition of endosperm proliferation producessmall seeds with small embryos. We have manipulated endospermproliferation and seed size using a variety of methods, includingmodifications to the ratio of paternally to maternally inheritedchromosomes in the endosperm, cytosine methylation status of the parentscontributing to the seed, and use of the fis3/fie mutation (Scott etal., 1998; Adams et al., 2000; Vinkenoog et al., 2000). In theseexperiments we considered the resultant changes to seed growth to be‘endosperm-led’, and effects on the embryo and the seed coat to beindirect. Some of our experiments specifically ruled out a direct effecton seed coat growth because the seed parent was wild-type and only thefertilization products were directly modified: for example, in the caseof wild-type diploid seed parents crossed with tetraploid pollenparents, which produce large seeds (Scott et al., 1998), or wild-typeseed parents crossed with pollen parents hypomethylated by a DNAMETHYLTRANSFERASE 1 antisense construct, which produce small seeds(Adams et al., 2000). Similarly, Garcia et al. (2003) described thehaiku mutants of Arabidopsis thaliana, which produce small seeds due toearly arrest of endosperm proliferation. The authors also noted afailure of cell elongation after fertilization in the integuments ofhaiku mutants, and concluded this was an indirect effect of limitedendosperm growth.

3b Role of Integuments/Seed Coat in Establishing Seed Size

Alonso-Blanco et al. (1999) investigated seed size in wild-type plantsof two Arabidopsis thaliana accessions, Cvi and Ler: seeds of the formerweigh 80% more than seeds of the latter and are 20% longer. In bothaccessions, the authors found that ‘seed coat and endosperm growthpreceded embryo growth, determining the overall final length of theembryo and the seed’. They did find that the outer layer of the matureseed coat has more cells in Cvi than Ler, but did not investigate orcomment on whether these extra cells were formed before or afterfertilization. Moreover, the authors' inspection of mature unfertilizedovules showed that ovules in Ler were slightly longer than in Cvi, andtherefore the authors concluded that ‘ovule size differences could notaccount for the final Ler/Cvi seed size variation’. Their overall majorconclusion was that ‘the larger size of Cvi seeds compared with Ler ismainly because of the faster and prolonged growth of the integuments andthe endosperm’ (i.e. after fertilization); they did not address thequestion of whether this growth was led by the integuments or theendosperm. The authors suggested that the final cell number and size inthe seed coat ‘may be determined during ovule development’, butsignificantly, there was no suggestion that a larger number ofintegument cells before fertilization was responsible for a larger finalseed size.

Garcia et al. (2005) examined crosses between Arabidopsis mutant ortransgenic plants that produce small seeds because of the inhibition ofeither endosperm growth or integument/seed coat growth. These authorsproposed a model in which seed size is determined by a reciprocalinteraction between endosperm growth and elongation of integument/seedcoat cells. They also reported that genotypes with fewer cells in theintegument compensate by increasing cell elongation. The authorsconcluded, ‘The final cell number in the integument [seed coat] isbalanced by cell elongation and does not influence the size of theseed.’

Jofuku et al. (2005) and Ohto et al. (2005) reported that mutations inthe APETALA2 (AP2) gene increase seed size; Jofuku et al. (2005) alsofound that suppression of AP2 activity through antisense or sensecosuppression had the same effect. ap2 mutant seeds have seed coatabnormalities including large and irregular outer integument cells, lackof mucilage, and hypersensitivity to bleach; and the increase in seedsize was found to be a mainly (Jofuku et al., 2005) or wholly (Ohto etal., 2005) maternal effect. However, neither paper investigated anypossible correlation between (1) seed size and (2) cell number or anyother aspect of integument/seed coat morphology in ap2 mutants ortransgenics.

Weber et al. (1996) compared growth of the seed coat in large- andsmall-seeded genotypes of Vicia faba (broad bean). They found thatlarge-seeded genotypes contained more cells in the seed coat at 9 daysafter pollination, but cell numbers in the two genotypes were similar at4 days after pollination. Therefore the number of cells in theinteguments before fertilization could not be a factor in final seedsize.

4. Relevant Patent Publications

(i) Fischer and Mizukami (2003), ‘Methods for altering organ mass inplants’, US Patent Application 20030159180

Mutations in the AINTEGUMENTA (ANT) gene of Arabidopsis thaliana preventformation of the integuments (Klucher et al., 1996; Baker et al., 1997).Mizukami and Fischer (2000) describe the phenotype of Arabidopsisthaliana plants over-expressing the wild-type ANT gene under the controlof the constitutive 35S promoter. Ectopic ANT expression increases thesize of many plant organs including seeds, as well as causing malesterility through failure of anther dehiscence. Most of the transgenicplants are also female sterile ‘because of abnormally extendedproliferation of the chalazal nucellar cells’. However weakoverexpressers could generate seeds after hand-pollination withwild-type pollen. ‘The enlarged 35S: ANT fruit included T2 seeds thatwere larger than normal (not shown in the application), because ofenlarged embryos.’ The size of unpollinated ovules, and the number orsize of cells in the integuments/seed coat, were not investigated ordiscussed. The large seed size of 35S::ANT seeds was attributed only tosize of the nucellus and embryo. US patent application no. 20030159180describes uses of a modified ANT polypeptide for altering the size ofplant organs including seeds. It was reported that the transgenic plantshad varying degrees of fertility that were not correlated with organsize. There was no investigation of the effect of expressing themodified ANT polypeptide on integument or seed coat growth.

(ii) Jofuku and Okamuro (2001), ‘Methods for improving seeds’, U.S. Pat.No. 6,329,567

Mutations in the APETALA2 (AP2) gene increase seed size (Okamuro andJofuku, 1997). The mutations have a maternal effect on seed size but theonly phenotype described for the integument/seed coat in ap2 mutants isthat the cells of the outer layer of the seed coat are enlarged with anirregular shape, along with some other morphological abnormalities(Jofuku et al., 1994). U.S. Pat. No. 6,329,567 describes methods ofmodulating seed mass using AP2 transgenes, but this patent does notassess any effect of the transgenes on the integuments or seed coat.

(iii) Lepiniec et al. (2003), ‘Regulating Nucleic Acid for Expressing aPolynucleotide of Interest Specifically in the Endothelium of a PlantSeed and Uses Thereof’, WO 03/012106 A2

The BANYULS (BAN) gene is expressed exclusively in the inner layer ofthe inner integument (this layer is also called the endothelium) inearly seed development (pre-globular stage) (Devic et al., 1999).International patent application WO 03/012106 A2 describes use of theBAN promoter to drive expression of various genes specifically in thetesta (the seed coat layer derived from the inner integument). Theauthors propose uses such as modifying the tannin or fibre composition,or the hormonal equilibrium, but no relevant expression cassettes werereported or described. Modification of seed size is also proposed butonly in the context of reducing or ablating seeds in fruit crops. A BANpromoter::BARNASE construct was shown to ablate the endothelium.

(iv) Zinselmeier et al. (2000), ‘Regulated Expression of Genes in PlantSeeds’, WO00/63401

This patent application relates to expression of genes such as ipt that‘affect metabolically effective levels of cytokinins in plant seeds, aswell as in the maternal tissue from which such seeds arise, includingdeveloping ears, female inflorescences, ovaries, female florets,aleurone, pedicel, and pedicel-forming regions’, and to transgenicplants with enhanced levels of cytokinin that exhibit ‘improved seedsize, decreased tip kernel abortion, increased seed set duringunfavorable environmental conditions, and stability of yield’. Anucellus promoter (nucellus is the maternal tissue surrounding theembryo sac and enclosed within the integuments) is among those suggestedfor driving expression cassettes, but integuments are not specificallymentioned in the patent application, nor were any maternaltissue-specific expression cassettes described. The disclosure of thispatent application is particularly concerned with maize.

(v) Scott (2002), ‘Modified plants’, WO/0109299

This patent application relates to methods for controlling endospermsize and development through use of an antisense DNA METHYLTRANSFERASE 1gene that reduces cytosine methylation. As described in WO01/09299, andin Section 3a, above, modification to the cytosine methylation status ofthe seed or pollen parent alters seed size by altering the rate andextent of endosperm proliferation. Therefore the disclosure of thispatent application relates exclusively to ‘endosperm-led’ seed growth.

In summary, documents in the prior art do not include an understandingthat altering the size of integuments specifically through increasingthe number of cells before fertilization could affect seed size afterfertilization. A small number of published papers and patentapplications touch on a possible relationship between seed coat size andseed size but do not make a link between (1) integument growthpre-fertilization and (2) final seed size.

5. Integument-Led Seed Growth

We were surprised therefore to discover in our laboratory a mutant,termed the mnt-1 mutant, that produces enlarged seeds through a primaryeffect on the integuments. Specifically, we observed that the seedcavity (i.e. the space within the post-fertilization embryo sac) islonger than normal giving the embryo more space to grow as a result ofan increase in cell number in the integument. This was particularlysurprising in view of the earlier research mentioned in section 3 aabove which indicated that changes in seed growth were ‘endosperm-led’.It was also surprising in view of the work of Alonso-Blanco et al (1999)mentioned in section 3b above which did not suggest that an increase innumber of integuments cells led to an increase in seed size; and also inview of the work of Weber et al 1999 who found similar numbers of cellsin the seed coat in small and large-seeded genotypes of broad bean soonafter fertilization; and also in view of the work of Garcia et al.(2005) who claimed that ‘The final cell number in the integument [seedcoat] is balanced by cell elongation and does not influence the size ofthe seed’; and also in view of the work of Jofuku et al (2005) and Ohtoet al. (2005) who found a maternal effect of the ap2 mutation on seedsize but did not report a correlation between cell number in theinteguments or in the seed coat and final seed size.

6. Increased Stem Diameter in mnt-1 Mutants

Increased stem diameter is also desirable in agriculture, as it may leadto an increase in plant biomass, which may in turn increase yield(Reynolds et al., 2001). Increased stem diameter and biomass are alsodesirable in certain crops such as trees and vegetables. Thicker stemsare also desirable because this trait increases resistance to lodging, aserious problem that reduces yields in crops including cereals (Zuber etal., 1999), soybean (Board, 2001), and oilseed rape (Miliuviene et al.,2004). A further aspect of the mnt-1 mutant phenotype is increaseddiameter of the stems.

DEFINITIONS

The following non-limiting definitions of terms used in thisspecification are given by way of explanation.

“Function” when used in relation to a gene embraces both the operationof that gene at a molecular level as well as the downstream effects ofexpression of the gene which may result in phenotypic changes.

“Nucleic acid sequence”: refers to a single or double-stranded polymerof deoxyribonucleotide or ribonucleotide bases read from the 5′ to the3′ end, including chromosomal DNA, plasmids, infectious polymers of DNAor RNA and DNA or RNA that performs a primarily structural role.

“Orthologues”: refers to genes derived from a common ancestral gene andwhich are found in different species as a result of speciation. Genesfound in different species are considered orthologues when theirnucleotide sequences and/or their encoded protein sequences have a highpercentage of sequence identity and/or similarity. Functions oforthologues are often highly conserved among species.

“Homologue”: A gene (or protein) with a similar nucleotide (or aminoacid) sequence to another gene (or protein) in the same or anotherspecies.

“Promoter”: a region or sequence located upstream and/or downstream fromthe start of transcription involved in recognition and binding of RNApolymerase and other proteins to initiate transcription.

“Plant promoter” refers to a promoter capable of initiatingtranscription in plant cells.

“Operably linked” refers to a functional linkage between a promoter anda DNA sequence, wherein the promoter sequence initiates and mediatestranscription of the DNA sequence. Generally, “operably linked” meansthat the nucleic acid sequences being linked are contiguous, and, wherenecessary to join two protein coding regions, contiguous and in the samereading frame.

“Plant”: includes whole plants, plant parts, and plant propagativematerial including: shoot vegetative organs and/or structures (e.g.leaves, stems and tubers), roots, flowers and floral organs (e.g.bracts, sepals, petals, stamens, carpels, anthers), ovules (includingegg and central cells), seed (including zygote, embryo, endosperm, andseed coat), fruit (e.g., the mature ovary), seedlings, plant tissue(e.g., vascular tissue, ground tissue), cells (e.g., guard cells, eggcells, trichomes and the like), and their progeny.

“Plant cell”: includes cells obtained from or found in seeds, suspensioncultures, embryos, meristematic regions, callus tissue, leaves, roots,shoots, gametophytes, sporophytes, pollen, and microspores as well aswhole plants. The term “plant cells” also includes modified cells, suchas protoplasts, obtained from the aforementioned tissues.

“Wild type” in the context of a plant or plant material which has beenmodified in some way refers to a comparable plant which has not beenmodified in that way and grown or produced under similar conditions. Fora given plant it may be the genotype or phenotype that is found innature or in standard laboratory stock. References in this specificationto relative changes in characteristics of plants or plant material arerelative to wildtype.

SUMMARY OF THE INVENTION

According to one aspect, the invention provides a method of modifyingcell proliferation in a plant which comprises modulating the expressionof a gene whose expression or transcription product is capable ofdirectly or indirectly modulating cell proliferation in the plant orplant propagating material, whereby cell proliferation, within theinteguments and/or seed coats of the plant, is modified. Cellproliferation in other parts of the plant may also be modified. Forexample, in the stem of the plant.

According to another aspect, the present invention provides a method ofmodifying cell proliferation in a plant which comprises the step oftransforming a plant or plant propagating material with a nucleic acidmolecule comprising at least one regulatory sequence, typically apromoter sequence, capable of directing expression within theinteguments and/or seed coat of at least one nucleic acid sequence whoseexpression or transcription product is capable of directly or indirectlymodulating cell proliferation, whereby, on expression of that sequence,cell proliferation is modified. Preferably, the overall size of theinteguments/seed coat in the plant is modified. This may be useful wherea product is produced in the integument/seed coat. In some embodiments,this will be achieved without affecting the growth or development of anypart of the plant other than the seed.

In one embodiment, the function of a gene or gene product that promotescell division is enhanced or the function of a gene or gene product thatrepresses cell division is inhibited. Cell division in theinteguments/seed coat may be increased resulting in a larger seedcompared to wild type. This may be advantageous because increases inseed size can be achieved which are desirable as mentioned above. Theseed may be at least 15%, or 25%, larger than wild type. Morespecifically, the seed may be at least 5%, 10%, 20%, 30%, 40%, 50%, 75%,100%, 150%, or even 200% heavier than wild-type. The number of cells inthe integuments/seed coat of the plant may be increased compared to wildtype. The number of cells in the integuments/seed coat of the plant maybe increased by at least 30%, or 50%, compared to wild type.

The diameter of the stem of the plant may be greater, for example atleast 10% greater, than wild type. Preferably, the diameter of the stemof the plant is at least 20% greater than wild type. This may beadvantageous as discussed above.

The sepal length of the plant may sufficiently greater than wild type toinhibit flower opening. For example, the sepal length may be at least20%, or at least 50% greater than wild type.

Equally, the method allows the production of smaller seeds which canalso be advantageous as mentioned above, and in another embodiment, thefunction of a gene or gene product that promotes cell division isinhibited or the function of a gene product that represses cell divisionis enhanced. Cell division in the integuments/seed coat may decreasedresulting in a smaller seed compared to wild type. The seed may be atleast 5% smaller than wild type, preferably 25% or more. The number ofcells in the integuments/seed cost may be decreased compared to wildtype. In particular the number of cells in the integuments/seed coat maybe reduced by at least 30%, or 50%, compared to wild type.

The function of a gene that modulates cell proliferation may be enhancedcompared to wildtype. Transcription of the gene is activated. Activationof transcription results in increased levels of mRNA and/or proteinencoded by the gene. Typically, levels of mRNA may be increased by atleast 20%. For example, the levels of mRNA may be increased by 50% or75% or more.

A plant promoter may be operably linked to a coding region of the genein the sense orientation. The function of the gene may be modulated byoperably linking a plant promoter to a nucleic acid fragment from thegene to form a recombinant nucleic acid molecule such that an antisensestrand of RNA will be transcribed.

The function of a gene may be modulated by introducing a nucleic acidfragment of the gene into an appropriate vector such thatdouble-stranded RNA is transcribed where directed by an operably linkedplant promoter. Decreased levels of mRNA and/or protein encoded byendogenous copies of the gene may be produced. Levels of mRNA andprotein encoded by homologues of the gene may be reduced.

The function of the gene may be modulated by operably linking a plantpromoter to a ‘dominant negative’ allele of the gene, which interfereswith the function of the gene product.

The plant may be monocotyledonous, and is preferably a crop plant. Forexample, the plant may be Tritcum spp (wheat), Oryza sativa (rice), Zeamays (maize), Hordeum spp. (barley), Secale cereale (rye), Sorghumbicolor (sorghum), or Pennisetum glaucum (pearl millet). Alternativelythe plant is dicotyledonous. For example, the plant is Brassica napus(oil seed rape, canola) or any other Brassica species used to produceoilseeds (e.g. Brassica carinata), Glycine max (soybean), Arachishypogaea (peanut), Helianthus annuus (sunflower), Phaseolus vulgaris(e.g. kidney bean, white bean, black bean), Vicia faba (broad bean),Pisum sativum (green pea), Cicer arietinum (chick pea), Lens culinaris(lentil), or Linum usitatissimum (flax, linseed).

Integument and seed coat development is similar in all species examinedin the family Brassicaceae (Bouman, 1975), to which Arabidopsis thalianabelongs. In Brassica napus, a crop plant closely related to Arabidopsisthaliana, the seed coat is also very similar in structure (Wan et al.,2002). Therefore modifications that affect growth and development ofinteguments/seed coat in Arabidopsis thaliana should be directlyapplicable to members of the Brassicaceae, including Brassica napus.

The mature seeds of monocots such as cereals have a distinct structure.However cereal ovules have fundamental similarities with ovules ofArabidopsis thaliana and other dicots, also consisting of integumentsenclosing a nucellus and embryo sac.) In rice, for example, the innerintegument encloses the ovule before fertilization, and its growthprecedes that of the endosperm and embryo, as in Arabidopsis thaliana(Lopez-Dee et al., 1999). Therefore modification to growth of theinteguments/seed coat may also be effective in altering overall seedgrowth in cereal crops. Specifically in rice a modification to growth ofthe inner integuments may be useful in modifying seed size.

It is notable that the INO gene, which in Arabidopsis thaliana isexpressed in the outer integument and required for its growth(Villanueva et al., 1999), has been identified in Nymphaea alba (waterlily), where it is also expressed in the integuments (Yamada et al.,2003). As the Nymphaeaceae are basal eudicots, which are ancestral toboth dicots and monocots, this suggests that the sequence and expressionpatterns of at least some integument genes will be conserved even amongdistantly related groups of flowering plants.

The present invention is complementary to the invention disclosed inWO01/09299. Modifications to endosperm-led and integument-led seedgrowth could be combined for an even larger effect. In some situationsintegument-led seed growth alone may be preferable, as it only requiresmodification to the seed parent, while endosperm growth is determinedboth by maternal and paternal contributions.

Where the regulatory sequence is a promoter, the promoter sequence maybe constitutive, directing gene expression in most or all cells of theplant. An example of a constitutive promoter that may be used in someembodiments of the invention is the 35S promoter, derived from the genethat encodes the 35S subunit of Cauliflower Mosaic Virus (CaMV) coatprotein. Alternatively, the promoter sequence may be specific, directingexpression exclusively or primarily in one organ, tissue, or cell typeof the plant. A variety of plant promoters can be used in the inventionto direct expression exclusively or primarily in the integuments or seedcoat. Suitable plant promoters include those obtained from plants, plantviruses, and bacteria which comprise genes expressed in plant cells,such as Agrobacterium or Rhizobium. Some embodiments use promotersexpressed in the pre-SUBSTITUTE fertilization integuments. These includebut are not restricted to the promoters of the following genes: INO(Villanueva et al., 1999; At1g23420, accession no. AF195047) and BEL1(Reiser et al., 1995; At5g41410; accession no. NM_(—)123506). Otherembodiments use promoters expressed in the seed coat afterfertilization. These include but are not restricted to the promoters ofthe following genes: BAN (Devic et al., 1999; At1g61720, accession no.AF092912), TT1 (Sagasser et al., 2002), TT2 (Nesi et al., 2001;At5g35550; accession no. NM_(—)122946), TT8 (Nesi et al., 2000;At4g09820, accession no. AJ277509), TT12 (Debeaujon et al., 2001;At3g59030, accession no. AJ294464), and TT16 (Nesi et al., 2002;At5g23260; accession no. NM_(—)203094). A flower-preferred promoter thatmay be used is the promoter of the LFY gene (Weigel et al., 1992;At5g61850, accession no. NM_(—)125579), which can be used to obtaindesired flower-specific effects such as reductions in flower opening.Where a promoter is to be introduced into a plant, a promoter-containingnucleotide sequence of up to 2000 bp would typically be used.

The use of other regulatory sequences than a promoter to directexpression within the integuments and/or seed coat is contemplated. Anexample is an intron directing tissue-specific expression (see e.g.Deyholos and Sieburth, 2000).

There are a number of genes known or suspected to be involved inmodulating cell proliferation, either directly or indirectly. Someembodiments of the invention use genes involved in hormone response,biosynthesis, translocation, or other aspects of hormone action. Theseinclude but are not restricted to MNT (described above), IPT1 (Takei etal., 2001; At1g68460, accession no. AB062607), and ARGOS (Hu et al.,2003; At3g59900, accession no. AY305869). Other embodiments use corecell cycle genes (Vandepoele et al., 2002). These include but are notrestricted to CYCD3;1 (formerly Cycδ3; Soni et al., 1995; Vandepoele etal., 2002; At4g34160, accession no. X83371) and CYCB1;l (formerlyCyc1aAt; Ferreira et al., 1994; Vandepoele et al., 2002; At4g37490,accession no. NM_(—)119913). Other embodiments use transcription factorsinvolved in regulation of the extent or rate of cell proliferation.These include but are not restricted to ANT (Klucher et al., 1996;At4g37750, accession no. NM_(—)119937).

An expression cassette may be used either to enhance or inhibit thefunction of a gene that modulates cell proliferation.

One method of enhancing function is to activate transcription of thegene, resulting in increased levels of mRNA and protein encoded by thegene. This is achieved by linking a plant promoter to the coding regionof the gene (either with or without introns) in the sense orientation.

Partial or complete inhibition of gene function in order to achievedesirable characteristics in plants such as fertility may be achieved or“engineered” in several ways. One method, which uses ‘antisensetechnology’, is to link a plant promoter to a nucleic acid segment fromthe desired gene such that the antisense strand of RNA will betranscribed (see e.g. Branen et al., 2003; Choi et al., 2003). Anothermethod, which uses ‘RNAi technology’, is to link a plant promoter to anucleic acid segment from the desired gene and place the resultingrecombinant nucleic acid into an appropriate vector such thatdouble-stranded RNA is transcribed (Wang and Waterhouse, 2001). Both ofthese techniques may result in decreased levels of mRNA and proteinencoded by the endogenous copies of the gene. For example, levels ofmRNA may be reduced by at least 20%, preferably by at least 50% so as toachieve usefully large seeds without compromising fertility compared towildtype. A nucleic acid fragment for antisense or RNAi technology mayalso be designed to decrease levels of mRNA and protein encoded byhomologues or orthologues of the gene. A third method of inhibiting genefunction is to link a plant promoter to a ‘dominant negative’ allele ofthe gene, which interferes negatively with the function of the geneproduct (see e.g. Hemerly et al., 1995; Nahm et al., 2003). In the caseof inhibition of genes (e.g., by antisense, or the use of RNAitechnology) it will be recognized that the inserted polynucleotidesequence need not be identical, but may be only “substantiallyidentical” to a sequence of the gene from which it was derived.Inhibition of gene function may be achieved by reduction of expressionof the gene through a feedback loop acting on that expression.

Alternatively, the nucleic acid sequence is a mutant form of an auxinresponse factor encoding gene, or a construct that inhibits expressionor function of an auxin response factor. The auxin response factor genemay be MNT in the case of Arabidopsis thaliana or its orthologues inother species. For example, in the case of Brassica napus the gene maybe BnARF2 as used in Example 2 below. In the case of rice the gene maybe OsARF2. The mnt-1 mutant phenotype shows that the wild-type functionof the MNT gene is to repress cell division in the integuments.Therefore inhibition of endogenous MNT expression or function may resultin larger integuments and a larger seed. Alternatively, enhancement ofMNT expression or function may result in a smaller seed. In somesituations, overexpressing the MNT gene may, in fact, result in a largerseed size possibly due to a feedback loop on the expression of the MNTgene.

In some embodiments of the invention, cell division in theinteguments/seed coat will be increased, resulting in a larger seedcompared to wild type. This may be achieved by enhancing function of agene or gene product that promotes cell division, or inhibiting functionof a gene or gene product that represses cell division. In otherembodiments, cell division in the integuments/seed coat will bedecreased, resulting in a smaller seed. This may be achieved byenhancing function of a gene or gene product that represses celldivision, or inhibiting function of a gene or gene product that promotescell division. In these embodiments the gene or gene product may be MNTor an orthologue of MNT; alternatively it may be another gene or geneproduct that affects cell division.

A plant may be further modified to maintain desirable characteristicsmay have been otherwise lost as a result of the transformation step. Forexample, the desirable characteristic may be fertility.

The plant may be engineered or bred further to maintain or introducedesirable characteristics. For example, the plant may be bred so that itis heterozygous for the modulated gene which directly or indirectlymodifies cell proliferation. In particular, we have found that plantsheterozygous for the mnt mutation have normal flowers and normalfertility, but that their seeds that are consistently significantlyheavier than wild-type (typically about 10-20%), though not as heavy asseeds from mnt homozygous mutants. In other words, if MNT function isreduced by about 50% rather than abolished completely, the plantsproduce desirable heavier seeds without compromising fertility. Forexample, plants may be engineered as described above in order to reducemRNA/protein levels for the cell proliferation gene.

For example, in further embodiments of the invention, MNT function isrestored to petals and stamens of an mnt mutant such that seeds have theenlarged mnt-1 mutant phenotype but fertility is not impaired. This maybe achieved by operably linking the promoter of a gene that directsexpression in petals and stamens but not carpels (which contain theovules), such as AP3 (Jack et al., 1992), to the wild-type MNT gene. Indifferent species, different wild type genes may be supplied. In otherembodiments, MNT function may be restored to sepals and petals of an mntmutant such that seeds have the enlarged mnt-1 mutant phenotype butfertility is not impaired. This may be achieved by operably linking thepromoter of a gene that directs expression in sepals and petals but notcarpels, such as AP1 (Mandel et al., 1992), to the wild-type MNT gene.In different species, different wild-type genes may be supplied.

According to another aspect of the invention there is provided a plantwhich includes a nucleic acid molecule comprising at least oneregulatory sequence capable of directing expression within theinteguments and/or seed coat of at least one nucleic acid sequence whoseexpression or transcription product is capable of directly or indirectlymodulating cell proliferation, whereby, on expression of that sequence,cell proliferation is modified. The plant may have been obtained by amethod in accordance with the invention and will have the resultingfeatures in terms of genetic structures and phenotype as set out in anyof claims 76 to 156 and/or described above.

According to a further aspect of the invention there is providedreproducible or propagatable plant material including a nucleic acidmolecule comprising at least one regulatory sequence capable ofdirecting expression within integuments and/or seed coat and at leastone nucleic acid sequence whose expression or transcription product iscapable of directly or indirectly modulating cell proliferation, wherebyon expression of that nucleic acid sequence cell proliferation ismodified.

According to another aspect of the invention, there is provided a methodof modifying cell proliferation in a plant which comprises the step ofmodulating the response of the plant to an auxin whereby the overallcell number of the integuments/seed coat of the plant is modified. Theresponse to an auxin may be modified by altering the expression of anauxin response factor. Preferably, the auxin response factor is ARF2.The function of a gene encoding the auxin response factor may bemodulated so as to affect the function of the factor. In the case ofArabidopsis thaliana, the gene may be MNT. In the case of Brassica napusthe gene may be BnARF2. In the case of rice the gene may be OsARF2.Orthologues of these genes may be used in other species.

Most preferably, the function of an endogenous auxin response factorencoding gene is modulated for example by RNAi technology as describedabove. Most preferably, the function of that gene in theinteguments/seed coat is affected.

In a further aspect of the invention, there is provided a method ofmodifying the function of a gene that directly or indirectly modulatescell proliferation, such as MNT, in a plant such that the seeds areenlarged but characteristics such as flower opening and/or fertility,preferably both flower opening and fertility, are not impaired. Theseeds may be at least 10% or 20% larger than wild type. This may beachieved by breeding a plant that is heterozygous for a mutation in thegene such as MNT or an orthologue of that gene in other species. Inanother embodiment the plant has a partial loss-of-function mutation ina gene the function of which affects cell proliferation, such as MNT oran orthologue in other species. In another embodiment, the level of theRNA of that gene and protein is reduced in a wild-type plant by 30%,40%, 50%, or 60%, for example by operably linking a promoter, such asthe constitutive 35S promoter, to a nucleic acid fragment from the geneto form a recombinant nucleic acid molecule such that an antisensestrand of RNA will be transcribed; or to nucleic acid fragments of thegene in an appropriate vector such that double-stranded RNA istranscribed.

According to a further aspect, the present invention provides a methodof modifying cell proliferation in a plant which comprises the step oftransforming a plant or plant propagating material with a nucleic acidmolecule comprising at least one regulatory sequence, typically apromoter sequence, capable of directing expression within the stem of atleast one nucleic acid sequence whose expression or transcriptionproduct is capable of directly or indirectly modulating cellproliferation, whereby, on expression of that sequence, cellproliferation is modified. Preferably, the overall size of the stems inthe plant is modified. The stem may be at least 10%, 20%, 30%, or 40%greater in diameter than wild-type. In one embodiment of the invention,MNT function, or that of an orthologue, is at least partially inhibitedin the stem, for example by operably linking a promoter such as theconstitutive 35S promoter to a nucleic acid fragment from the MNT geneor MNT orthologue to form a recombinant nucleic acid molecule such thatan antisense strand of RNA will be transcribed; or to nucleic acidfragments of the MNT gene or MNT orthologue in an appropriate vectorsuch that double-stranded RNA is transcribed.

In another embodiment of the invention, the function of a gene thatdirectly or indirectly modulates cell proliferation such as MNT or anorthologue thereof is restored to flowers of an mnt mutant such thatstems have the enlarged mnt-1 mutant phenotype but fertility is notimpaired. This may be achieved for example by operably linking thepromoter of a gene that directs expression in flowers but not stems,such as LEAFY (LFY) (Weigel et al., 1992; At5g61850, accession no.NM_(—)125579), to the wild-type MNT gene. In different species,different wild type genes may be supplied.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments in accordance with the invention will now be described, byway of example only, with reference to the accompanying drawings FIGS. 1to 25 in which:

FIG. 1A Top: Confocal micrographs of seeds with globular stage embryosfrom mnt-1 (left) and wild-type (right) seed parents; Bottom: Matureseeds and embryos from mnt-1 mutants and wild-type plants, photographedat the same scale;

FIG. 1B is a scatter plot of number of seeds in each pod produced bymnt-1 mutants vs mean seed weight in that pod, following controlledpollinations;

FIG. 1C shows seeds from manually pollinated mnt-1 and wild-type plants,and reciprocal crosses between them, photographed at the same scale;

FIG. 2A shows light micrographs of mature unfertilized ovules, stage3-VI (staging as in Schneitz et al., 1995), from wild-type (left) andmnt-1 (right) plants;

FIG. 2B shows graphs showing number of cells, total length, and meancell length for several integument layers in mnt-1 and wild-type stage3-VI ovules. (The width is also shown for layer ii1′).

FIG. 3 shows micrographs of the chalazal endosperm in developing seedsof Arabidopsis thaliana, all at the same scale. The mnt-1 seed is anexample of integument-led growth while the 2x×6x seed provides anexample of endosperm-led growth;

FIG. 4A shows micrographs of Arabidopsis thaliana seeds illustratingendosperm-led seed growth illustrated by interploidy crosses in the C24accession of Arabidopsis thaliana (see also Scott et al., 1998);

FIG. 4B shows micrographs illustrating integument-led seed growthillustrated by the mnt-1 mutant in the Columbia accession of Arabidopsisthaliana;

FIG. 4C is a micrograph of a seed illustrating the ‘big bag’ hypothesis;

FIG. 5A-C is a photograph illustrating a comparison of floral phenotypeand seed size in wild-type Col-3 (5A), mnt-1 mutants (5B), and a Salkinsertion mutant (Salk line 108995) homozygous for an insertion in theARF2 gene (5 C);

FIG. 5D is a photograph of a gel showing PCR-based scoring of segregantsfor the T-DNA insertion in Salk line 108995;

FIG. 5E is a photograph of a gel showing scoring of presence of theinsertion (top) and presence of homozygotes (bottom) in F1 progeny ofthe cross between an mnt-1 homozygous mutant seed parent and the Salk108995 homozygous pollen parent. All F1 progeny have a single copy ofthe insertion;

FIG. 5F is a photograph illustrating floral and seed phenotype in an F1hybrid plant resulting from a cross between a homozygous mnt-1 mutantand a homozygous Salk insertion mutant (Salk line 108995);

FIG. 6 is an alignment of wild-type MNT and mutant mnt-1 cDNAs fromtranslational start to stop;

FIG. 7 is an alignment of wild-type MNT and mutant mnt-1 predictedproteins;

FIG. 8 is an alignment of Arabidopsis thaliana a MNT cDNA with itsorthologue in Brassica napus, BnARF2;

FIG. 9 is an alignment of Arabidopsis thaliana MNT predicted proteinwith its orthologues in Brassica napus (oilseed rape) (BnARF2) and Oryzasativa (rice) (OsARF2);

FIG. 10 illustrates the BJ60, BJ40, pFGC5941, pART7, and BJ36 vectorsused for the cloning strategies described in the following examples;

FIG. 11 illustrates a cloning strategy for constructing reporter vectors(Example 3). In this and following figures, only restriction sitessignificant to the strategy are shown on the diagrams;

FIG. 12 is a micrograph of a globular stage seed from a plant containingthe TT12::uidA construct assayed for GUS expression; the inner layer ofthe inner integument is stained (arrow);

FIG. 13A illustrates a cloning strategy for constructing an RNAi vectorto constitutively decrease MNT expression (Example 4);

FIG. 13B is a series of photographs illustrating inflorescence and stemphenotypes (top) and seed sizes and weights (bottom) from independentlytransformed lines containing the 35S::MNT RNAi expression cassettecompared with a wild-type control. Inflorescences and stems werephotographed at the same scale, and seeds were photographed at the samescale;

FIG. 14 illustrates a cloning strategy for constructing an RNAi vectorto constitutively decrease BnARF2 expression (Example 5);

FIG. 15 illustrates a cloning strategy for constructing RNAi vectors todecrease MNT expression primarily in the integuments/seed coat (Example6);

FIG. 16 illustrates a cloning strategy for constructing RNAi vectors todecrease BnARF2 expression primarily in the integuments/seed coat(Example 7);

FIG. 17A illustrates a cloning strategy for constructing vectors forconstitutive expression of MNT (Example 8) or BnARF2 (Example 9);

FIG. 17B is a series of photographs illustrating seed sizes and weightsfrom independently transformed lines containing the 35S::MNT expressioncassette compared with a wild-type control. Seeds were photographed atthe same scale;

FIG. 18 illustrates a cloning strategy for constructing vectors forexpression of MNT in the integuments/seed coat (Example 10);

FIG. 19 illustrates a cloning strategy for constructing vectors forexpression of BnARF2 in the integuments/seed coat (Example 11);

FIG. 20 illustrates a cloning strategy for constructing vectors forexpression of genes promoting cell division in the integuments/seed coat(Examples 12, 13);

FIG. 21A is a series of photographs illustrating seed sizes and weightsfrom individual primary transformants containing expression cassettesdesigned to increase seed size (TT8::CYCD3;l and TT8::IPT1) comparedwith controls (TT8::uidA). Data is taken from Table 2A. Seeds werephotographed at the same scale;

FIG. 21B is a series of photographs illustrating seed sizes and weightsfrom transformed plants containing expression cassettes designed toincrease seed size compared with wild-type controls. Data is taken fromTable 2B. Seeds were photographed at the same scale;

FIG. 22 illustrates a cloning strategy for constructing a vector forexpression of MNT in petals and stamens (Example 14);

FIG. 23 illustrates a cloning strategy for constructing a vector forexpression of MNT in sepals and petals (Example 15);

FIG. 24A shows a wild-type Col-3 (left) and mnt-1 (right) plant,illustrating the stem phenotype;

FIG. 24B shows transverse sections of the inflorescence stem betweennodes 2 and 3 as counted from the base of a wildtype from a wild-type(top) and mnt-1 (bottom) plant. Each pair of images (low magnification,left; high magnification, right) was photographed at the same scale; and

FIG. 25 illustrates a cloning strategy for constructing a vector forexpression of MNT in flowers (Example 18).

DESCRIPTION OF PREFERRED EMBODIMENTS

Methods and products in accordance with the present invention will nowbe described with reference to the following examples, which should notbe construed as in any way limiting the invention.

The following vectors are used in the examples:

pGEMT (Promega, Southampton, UK)

BJ36, BJ40, BJ60 (gift of Bart Janssen, Horticultural & Food ResearchInstitute of New Zealand)

pART7 (Gleave, 1992)

pFGC5941 (Cambia, Canberra, Australia; ChromDB,http://www.chromdb.org/plasmids)

Plant transformation protocols are based on Clough and Bent (1998) forArabidopsis thaliana and Moloney et al. (1989) for Brassica.

Protein predictions and sequence alignments are carried out with GeneDocsoftware version 2.6.001 (Nicholas and Nicholas, 1997).

A. Identification of the mnt-1 Mutant

We identified the mutant, megaintegumenta-1 (mnt-1), in a screen forlarge seeds yielded by a population of EMS (ethylmethanesulfonate)-mutagenized Arabidopsis thaliana in theCol-3-accession. Mature seeds produced by a seed parent homozygous forthe mnt-1 mutation are larger and more pointed than wild-type, withextra cells in the seed coat, and contain larger embryos (FIG. 1A).Specifically, FIG. 1A shows that mnt-1 mutants produce larger seeds withmore cells in the seed coat (counts are for ii1, the outer layer of theinner integument).

Seeds collected from self-pollinated mnt-1 mutant plants are up to twicethe weight of wild-type Col-3 seeds (Table 1A).

TABLE 1A Seed weights in μg from mnt-1 and w.t. Col-3 crosses, selfseed, all siliques left on plant mnt self w.t. self 27.1 (n = 60) 14.4(n = 178) 27.9 (106) 15.8 (75) 29.7 (127) Mean 28.2 15.1 Range 27.1 to29.7 14.4 to 15.8 Standard error  0.8  1.4 n = number of seeds weighedfrom each plant

However, mnt-1 mutant plants are self-sterile until late in developmentdue to floral abnormalities (see below), raising the possibility thatthe mutant produces large seeds because there are few seeds requiringmaternal resources. Therefore we also conducted controlled pollinationsin which only three siliques (seed pods) were allowed to set seed perplant, for both mnt-1 and wild-type (Table 1B).

TABLE 1B Seed weights in μg from mnt-1 and w.t. Col-3 crosses, manualpollinations, 3 siliques per plant mnt × mnt mnt × w.t. w.t. × mnt w.t.× w.t. 31.1 (n = 32) 30.4 (n = 36) 30.5 (n = 20) 30.6 (n = 34) 37.7 (37)32.6 (22) 28.2 (30) 29.7 (34) 31.4 (37) 37.4 (43) 28.2 (32) 22.1 (49)  39 (20) 31.8 (17) 27.1 (46) 31.5 (31) 33.7 (50) 34.4 (33) 26.5 (44)29.6 (28) 40.5 (22)   36 (50)   28 (44) 26.9 (53) 38.3 (9)  37.1 (49)30.3 (44) 30.2 (61) 39.1 (11)   38 (24) 31.7 (48) 37.2 (25) 21.2 (32)35.2 (24) 35.7 (43)   39 (31) 38.3 (64)   34 (23) 36.1 (33) 35.1 (54)Mean 36.3 34.7 28.4 28.7 Range 31.1 to 40.5 31.8 to 38.0 26.5 to 30.522.1 to 31.7 Standard error  0.7  1.0  0.6  1.3 n = number of seeds insilique ttest [mnt × mnt] vs [w.t. × w.t.]: P < 0.000, significant ttest[mnt × mnt] vs [mnt × w.t.]: P > 0.2, not significant ttest [w.t. ×w.t.] vs [w.t. × mnt]: P > 0.9, not significant

This treatment raised the mean weight of wild-type seeds by 90% andmnt-1 seeds by 29%, indicating that low seed number is a component oflarge seed size in mnt-1 mutants but that the mnt-1 mutation also has asignificant effect. On average mnt-1 seeds weighed 26% more thanwild-type when only three siliques per plant set seed; the difference inweights was significant at P<0.000. We also investigated whetheroccasional low seed set within individual mnt-1 siliques might raiseseed weight; however a scatter plot (FIG. 1B) of mean seed weight ofeach pod vs number of seeds per pod following controlled pollinations inmnt-1 (data from Table 1B) shows no correlation.

We also compared the weight of seeds produced by mnt heterozygotes withthe weight of seeds produced by wild-type plants (Table 1C). Wegenerated the heterozygotes through crosses in both directions, i.e.[w.t. X mnt-1] (designated [wXm]) and [mnt-1× w.t.] (designated [mXw]).We found that the weights of seeds from w.t. and mnt-1 heterozygousplants were significantly different (t-test, Ho w.t.=mnt-1 heterozygous,P=0.0002).

TABLE 1C Seed weights in μg from w.t. Col-3 and mnt-1 heterozygousplants, self seed, all siliques left on plant w.t. mnt heterozygousPlant 1 17.1 (n = 35) 19.4 (n = 44) [w × m] Plant 2 16.5 (37) 20.8 (60)Plant 3 16.4 (49) 19.3 (50) Plant 4 16.2 (50) 18.8 (50) Plant 5 16.3(45) 19.5 (46) Plant 6 16.2 (40) 20.0 (62) Plant 7 15.3 (52) 19.3 (44)Plant 8 16.6 (42) 18.4 (59) Plant 9 17.5 (54) 18.7 (45) Plant 10 17.9(56) 18.3 (57) Plant 11 16.2 (64) [m × w] Plant 12 17.7 (67) Plant 1320.0 (42) Plant 14 17.3 (42) Plant 15 18.3 (75) Plant 16 17.1 (45) Plant17 17.0 (67) Plant 18 17.7 (49) Plant 19 18.3 (54) Plant 20 16.6 (40)Mean  16.6 (460)  18.4 (1062) Range 15.3 to 17.9 16.2 to 20.8 Standarderror 0.2 0.3

We also conducted two further experiments to compare the weights ofseeds from (a) wild-type plants, (b) mnt-1 homozygotes, and (c) mnt-1heterozygotes under conditions of restricted pollination. In the firstexperiment, six siliques on the primary shoot were pollinated and allother siliques on the primary shoot were removed; but all secondaryshoots were allowed to set self-seed (Table 1D). In the secondexperiment, only six siliques; on the primary shoot were pollinated andall other siliques on the plant were removed (Table 1E). In bothexperiments we carried out manual pollinations on six siliques per plantto enable young mnt-1 homozygous mutant plants to set seed.

TABLE 1D Seed weights in μg from w.t. Col-3, mnt-1 homozygous, and mnt-1heterozygous plants, 6 siliques pollinated on primary shoot, secondaryshoots allowed to self-pollinate w.t. mnt homozygous mnt heterozygousPlant 1 24.7 (n = 289) 35.5 (178) 31.0 (n = 237) [w × m] Plant 2 24.6(336) 34.5 (217) 28.7 (275) Plant 3 24.4 (337) 36.9 (224) 29.8 (140)Plant 4 23.9 (223) 37.8 (227) 30.7 (195) Plant 5 25.8 (135) 37.4 (149)29.3 (260) Plant 6 29.2 (109) [m × w] Plant 7 29.6 (307) Plant 8 29.0(198) Plant 9 26.8 (346) Plant 10 27.6 (341) Mean seed  24.7 (1320) 36.4(995)  29.2 (2408) weight Range 23.9 to 25.8 34.5 to 37.8 26.8 to 31.0Standard 0.3 0.6 1.3 error n = number of seeds weighed from each plantt-test: H₀ w.t. = mnt-1 homozygous, P < 0.0000, difference issignificant t-test: H₀ w.t. = mnt-1 heterozygous, P < 0.0000, differenceis significant

TABLE 1E Seed weights in μg from w.t. Col-3, mnt-1 homozygous, and mnt-1heterozygous plants, 6 siliques pollinated on primary shoot, secondaryshoots removed w.t. mnt homozygous mnt heterozygous Plant 1 33.0 (n =307) 38.7 (n = 274) 37.1 (n = 53) [w × m] Plant 2 32.2 (222) 37.5 (221)35.1 (300) Plant 3 35.1 (74)  41.1 (226) 37.7 (347) Plant 4 35.0 (252)41.0 (302) 35.6 (110) Plant 5 34.8 (230) 38.5 (205) 38.1 (195) Plant 640.9 (193) [m × w] Plant 7 37.8 (245) Plant 8 36.7 (280) Plant 9 38.1(210) Plant 10 39.9 (222) Mean seed  34.0 (1085)  39.4 (1228)  37.7(2155) weight Range 23.2 to 35.1 37.5 to 41.1 35.1 to 40.9 Standard 0.60.7 1.8 error n = number of seeds weighed from each plant t-test: How.t. = mnt-1 homozygous, P = 0.0004, difference is significant t-test:Ho w.t. = mnt-1 heterozygous, P = 0.0013, difference is significantmnt-1 homozygotes and mnt-1 heterozygotes produced heavier seeds thanwild-type plants in both experiments, and the difference in weight wassignificant in all cases at P<0.002. When secondary shoots were allowedto set seed, seeds from mnt-1 homozygotes were on average 47% heavierthan seeds from wild-type plants, and seeds from mnt-1 heterozygoteswere on average 18% heavier than seeds from wild-type plants. Whensecondary shoots were removed, so that only six siliques set on eachplant regardless of genotype, seeds from mnt-1 homozygotes weighed 16%more than wild-type, and seeds from mnt-1 heterozygotes weighed 11% morethan wild-type.

The mnt-1 mutation has a maternal effect on seed size. That is, an mnt-1homozygous mutant seed parent yields large seeds regardless of whetherit is pollinated by an mnt-1 or wild-type plant, while a wild-typeparent yields normal seeds even if pollinated by an mnt-1 plant (FIG.1C). In FIG. 1C seeds produced by mnt-1 seed parents are shown on topand seeds from wild-type seed parents are below. H=fertilizationproducts (embryo and endosperm) are heterozygous for the mnt-1 mutation.This shows that seed size in mnt-1 mutants depends on the genotype ofthe seed parent, not the fertilization products. This is also shown bythe lack of a significant difference between seed weights from [mnt-1×mnt-1] and [mnt-1× w.t] seeds, and between [w.t.×w.t.] and [w.t.×mnt-1]seeds (Table 1B).

The primary difference between mnt-1 and wild-type seeds is that themutant seeds contain more cells in the seed coat. Comparison of ovuledevelopment in mnt-1 and wild-type plants shows that mnt-1 ovules are ofnormal size and morphology until they are near maturity, at which timewe observe that both the inner and outer integuments of mnt-1 ovules aresignificantly longer than in wild-type, primarily due to a significantlygreater number of cells (FIG. 2). In relation to the results depicted inFIG. 2, in Arabidopsis thaliana and other members of the Brassicaceamost cell division and expansion occurs in the integuments on theabaxial side of the ovule (marked on wild-type ovule in FIG. 2A).Similarly, the nucellus in rice is enveloped by the abaxial innerintegument (Lopez-Dee et al., 1999). In Arabidopsis, ii1, ii1′, and ii2are the three cell layers of the inner integument and oil and oi2 arethe two layers of the outer integument. The cells of layer ii1′, whichdoes not completely span the embryo sac, significantly expand in widthafter fertilization as part of seed growth (Beeckman et al., 2000).mnt-1 ovules have longer integuments with extra cells and in some casesan extra layer (arrow), as well as a larger seed cavity (FIG. 2A). C=the‘curving zone’ of the abaxial outer integument (the region overlyingii1′; Beeckman et al., 2000), M=the ‘micropylar zone’, regions delimitedwith black bars (FIG. 2A). Measurements shown in FIG. 2B were taken forthe abaxial integuments only. Layers ii1′, ii1, and the curving zone ofoi2 are longer in mnt-1 mutant ovules, almost exclusively due to greatercell number. Mean cell length is greater in the micropylar zone of mnt-1ovules but smaller or not significantly different in the oi2 curvingzone and the other integument layers measured. There is no difference inmean width between mnt-1 and wild-type cells of layer ii1′.

The peripheral endosperm in mnt-1 mutant seeds also generates morenuclei than in wild-type seeds. The mean number of peripheral endospermnuclei in mnt-1 seeds at the heart stage is 1150, compared with 550 fora wild-type Col-3 seed at a comparable stage; see Scott et al. (1998)for a description of endosperm morphology and the counting method.However, we consider there are two crucial differences between mnt-1mutant seeds and large seeds that show endosperm-led growth. First, thechalazal region of the endosperm, which becomes greatly enlarged inendosperm-led seeds (e.g. seeds from interploidy crosses generatingpaternal excess, crosses where the DNA of the seed parent ishypomethylated, or fis mutants), is of roughly normal size in mnt-1mutants (although the pinched shape of the chalazal pole of mnt-1 seedsresults in a longer and narrower chalazal endosperm) (FIG. 3). Wemeasured the maximum cross-sectional area of the chalazal cyst plusnodules at 6 DAP, a stage at which differences are apparent betweenwild-type and paternalized endosperms (Scott et al., 1998). Mean areaswere 2690 μm² (±s.e.m. 328) for wild-type seeds (n=4) and 2537 μm²(±416) for mnt-1 seeds (n=5), and there was no significant differencebetween the mutant and wild-type endosperms (t-test, Ho w.t.=mnt-1,P=0.79). Second, the size difference between mnt-1 and wild-type seedsfollows from differences existing before fertilization i.e. before theendosperm has been created. The overproliferation of peripheralendosperm may follow from the larger seed volume created by enlargedinteguments/seed coat.

B. The ‘Big Bag’ Hypothesis

We observe that seeds with enlarged endosperms and seeds with large seedcoats have a feature in common: the seed cavity (i.e. the space withinthe post-fertilization embryo sac) is larger than normal, giving theembryo more space to grow (FIG. 4A, 4B). Specifically, endosperm-ledseed growth is illustrated by interploidy crosses in the C24 accessionof Arabidopsis thaliana (see also Scott et al., 1998). As shown in FIG.4A extra paternal genomes produce seeds with a large cavity (top left,2x×6x cross), and ultimately large seeds with large embryos (2x×4xcross, bottom left). Conversely, extra maternal genomes generate seedswith small cavities (top right, 6x×2x cross), and ultimately small seedswith small embryos (4x×2x cross, bottom right). The control 2x×2x crossis shown in the middle.

In contrast in integument-led seed growth as illustrated in FIG. 4B theseeds also have a large seed cavity (top left) compared with wild-type(top right). Mature seeds and embryos are compared below.

This leads to our ‘big bag’ hypothesis, which states that seed andultimately embryo size is set by the size of the seed cavity, which maybe controlled by several factors including extent of endospermproliferation and extent of integument/seed coat proliferation (FIG.4C).

It is well established in the literature that after fertilization inArabidopsis thaliana there is no further division in the seed coat, andgrowth occurs only by cell expansion (Leon-Kloosterziel et al., 1994;Beeckman et al., 2000; Windsor et al., 2000). Obviously seeds with largeendosperms must also have large seed coats; however, in this case, theseed coat grows by cell expansion after fertilization. In seeds wherelarge seed coat is considered the primary cause of seed enlargement(integument-led seed growth), the integument/seed coat contains extracells, as observed in mnt-1 mutants.

C. Further Aspects of the mnt-1 Mutant Phenotype

The mnt-1 mutation affects floral morphology as well as seed size. Mostflowers fail to open; this is associated with a deviation from thenormal ratio of sepal to petal length, so that the petals are shorterthan the sepals. Specifically, mnt mutant sepals are about 60% longerthan wild-type. This deviation is mainly due to overgrowth of the sepalscaused by extra cell division, although under some conditions the petalsalso fail to expand normally. This characteristic may be commerciallyuseful in some crop species. A smaller increase in sepal length may besufficient to prevent flower opening whilst allowing self-fertilization.Additionally, pollen is shed from the anthers on to the sides of thecarpel rather than the stigma. This is associated with overgrowth of thegynoecium caused by extra cell division, although under some conditionsthe stamen filaments do not extend normally.

The floral phenotypes result in sterility of plants unless manualpollination is carried out (mnt-1 homozygotes are female fertile, andthe pollen that completes development is also fertile). However the lastfew flowers produced by mnt-1 mutants appear wild-type and these areself-fertile.

Germination frequency of mnt-1 seeds is normal, and the seedlings arevigorous.

mnt-1 mutants have thick inflorescence stems compared with wild-typeplants (FIG. 24).A comparison of primary inflorescence stems shows thatmnt-1 stems have a 20% greater diameter than wild-type (mean diametersmnt-1, 1.59 mm±s.e.m. 0.04; w.t., 1.32 mm:±0.06; n=6 for each).Transverse sections (FIG. 24B) show that cells are of normal size inmnt-1 mutant stems but many more cells are formed.

D. Molecular Characterization of the Wild-Type mnt Gene and mnt-1 MutantAllele

i) Wild-Type mnt Sequence

We mapped the MNT locus to a 60.9 kb region of chromosome 5 that wasannotated by The Arabidopsis Information Resource (TAIR)(http://www.arabidopsis.org) to contain 17 genes. T-DNA insertion lineswith insertions in these genes generated by The Salk Institute GenomeAnalysis Laboratory (SIGnAL (Alonso et al., 2003)(http://signal.salk.edu) were obtained from the Nottingham ArabidopsisStock Centre (NASC) (http://nasc.nott.ac.uk). Salk line no. 108995 (NASCstock no. N608995), with an insertion in the coding region of the AUXINRESPONSE FACTOR 2 (ARF2) gene, included a plant homozygous for theinsertion with a similar phenotype to mnt-1 mutants, including closedflowers and large seeds (FIG. 5A-C). Genotypic scoring of segregantsfrom the Salk 108995 family, including one heterozygote and thehomozygote, is shown in FIG. 5D. Specifically in FIG. 5D Top: Scoringfor presence of an insertion in the ARF2 gene. Primers used were 5′ TGGTTC ACG TAG TGG GCC ATC G 3′, and 5′ GAG TGG GTG GAG TGT GTT TG 3′.Lanes M and O show presence of the insertion. Bottom: Scoring forhomozygous insertion mutants. Primers used were 5′ GAG TGG GTG GAG TGTGTT TG 3′ and 5′ AGT TGG TTT TCG TTT GAG CAT 3′. PCR conditions are setso that the gene will only amplify if there is no insertion: thereforePCR products will be amplified from DNA extracted from wild-type plantsand also those hemizygous for the insertion, but not homozygous plants.Lane M shows no amplification, indicating this plant is homozygous forthe insertion. An allelism test was conducted by crossing a seed parenthomozygous for the mnt-1 mutation with the Salk 108995 homozygote aspollen parent. F1 progeny were hemizygous for the insertion (FIG. 5E)and had the mnt-1 mutant phenotype (FIG. 5F), confirming that MNT is theARF2 gene.

MNT/ARF2 will be referred to as MNT in the remainder of this document.The MNT gene=At5g62000, accession no. NM_(—)125593. The genomic DNA forMNT, including the coding region plus 4371 bases of 5′ and 525 bases of3′ flanking region, is shown in SEQ ID NO. 1. SEQ ID NO. 2 is thecomplete cDNA, and SEQ ID NO. 3, the predicted protein.

ARFs form part of the system for responding to auxin, a hormone known tobe involved in many plant developmental processes including celldivision and expansion (Stals and Inzé, 2001; Leyser, 2002). ARFs aretranscription factors that in general are not induced by auxinthemselves but which regulate expression of auxin-inducible genes, suchas members of the Aux/IAA class (Liscum and Reed, 2002). ARFs have beenshown to bind to Auxin Response Elements (AREs) containing the motifTGTCTC in the promoters of auxin-inducible genes (Ulmasov et al.,1999a). Twenty-two ARFs predicted to be functional have been annotatedin the Arabidopsis thaliana genome (Hagen and Guilfoyle, 2002). ARFscontain two conserved domains—an N-terminal DNA binding domain and aC-terminal dimerization domain—and a variable middle region. An ARF mayactivate or repress transcription of its targets and this is thought todepend on the sequence of the middle region (Ulmasov et al., 1999b).Evidence so far suggests that ARF2 is likely to be a repressor (Tiwariet al., 2003).

ii) Mutant mnt-1 Sequence

We sequenced the coding region from genomic DNA of the mnt-1 allele plus4371 bases of the 5′ and 525 bases of the 3′ flanking regions (thisgenomic sequence is shown in SEQ ID NO. 4). A single base change withrespect to the wild-type Col-3 sequence, from G to A, was identified atposition 665 from translational start, at the end of intron 3. This waspredicted to affect splicing by changing the conserved 3′ splice site(Brown and Simpson, 1998) from the consensus AG sequence to AA. Wesequenced the first 837 bases of the mnt-1 cDNA from start oftranslation and confirmed that four bases are deleted from the beginningof exon 4. The mnt-1 cDNA from translational start to stop, consistingof the 837 directly sequenced bases plus the remainder of the cDNAcoding region as predicted from the sequenced mnt-1 genomic DNA, isshown in SEQ ID NO. 5. Wild-type MNT and mutant mnt-1 cDNA sequences arealigned in FIG. 6.

The predicted mnt-1 protein (SEQ ID NO. 6) has a frameshift from aminoacid position 123 and an early stop codon at position 167. Wild-type MNTand mutant mnt-1 predicted protein sequences are aligned in FIG. 7. Theframeshift and early stop codon are both within the DNA binding domainand therefore the mnt-1 allele is likely to cause a complete loss of MNTfunction.

Example 1 Value of mnt Mutants in Understanding and Modifying Growth ofInteguments/Seed Coat

The mnt mutant seed phenotype demonstrates that there is a correlationbetween the size of integuments before fertilization and the size of themature seed in Arabidopsis thaliana (FIGS. 1, 2). Due to thesimilarities in seed structure among even distantly related groups offlowering plants, this leads to the expectation that modification tointegument/seed coat size in other species, and certainly in members ofthe Brassicaceae such as Brassica napus, will also result in changes toseed size.

Our knowledge of the mnt mutant phenotype and MNT gene sequence can beexploited in other species through TILLING (‘Targeting induced locallesions in genomes’). In this reverse genetics technique, chemicallymutagenized populations are screened for presence of a point mutation ina nucleic acid sequence of interest; this can be done as ahigh-throughput procedure and is applicable to many species (Till etal., 2003). For example, TILLING could be applied to the Brassica napusor rice orthologues of MNT in order to modify seed size in these cropspecies.

Our knowledge that mnt-1 heterozygotes are self-fertile and producelarger seeds than wild-type plants shows that a plant with reduced MNTfunction (as in a heterozygote for an MNT mutation or in a plant whichhas been genetically modified in some way to achieve the same effect asconventional breeding) will advantageously produce large seeds without aloss of fertility.

Example 2 Modifying Expression of mnt Orthologues in Other Species

Knowledge of the MNT sequence in Arabidopsis thaliana also allows us tosearch for orthologues in crop species as a necessary first step intargeted modification of the expression of the gene in these species.

By way of example, we amplified the putative Brassica napus orthologue(BnARF2) of MNT using primers (SEQ ID NO 7, 8) based on the MNT sequenceand on publicly available Brassica oleracea sequence. The BnARF2 cDNAwas amplified from total RNA isolated from seedlings of Brassica napusvar. Westar. The BnARF2 cDNA from translational start to stop is shownin SEQ ID NO. 9 and is aligned with Arabidopsis thaliana MNT cDNA inFIG. 8. The BnARF2 predicted protein (SEQ ID NO. 10) has 85% identity toArabidopsis thaliana MNT.

A family of ARFs has also been characterized in rice and one of these,OsARF2 (accession no. AB071293), is considered to be the orthologue ofArabidopsis thaliana ARF2 (Sato et al., 2001). FIG. 9 shows an alignmentof the predicted protein sequences of MNT (Arabidopsis thaliana ARF2),BnARF2, and OsARF2.

Orthologues of MMT may be determined for other species using similartechniques.

Example 3 Construction, Transformation, and Analysis of Reporter Vectorsto Show where Integument/Seed Coat Promoters are Expressed inArabidopsis thaliana

This is to test which promoters are suitable for driving integument/seedcoat-specific or -preferred expression of nucleic acids such as MNTantisense or RNAi constructs, or other genes modifying cellproliferation.

Diagrams of the BJ60, BJ40, pFGC5941, pART7, and BJ36 vectors used inthe cloning strategies described in this and following examples areshown in FIG. 10.

The cloning strategy is shown in FIG. 11.

3a Construction of Reporter Vectors3a(i) TT8

A reporter vector based on the promoter of the TT8 gene (Nesi et al.,2000; At4g09820, accession no. AJ277509) is constructed as describedbelow. A 1.7 kb fragment including the TT8 promoter is amplified by thepolymerase chain reaction (PCR) from Arabidopsis thaliana genomic DNA 5′to translational start of the TT8 gene using the primers TT8F and TT8Rwhich introduce an NdeI and a PstI site at the 5′ and 3′ ends of the TT8PCR fragment respectively.

SEQ ID NO. 11 5′ AAACATATGCCAACGGGATCATGGGATTAC 3′ TT8F       NdeI SEQID NO. 12 5′ AAACTGCAGCGTTCCCGGAGATACGAAAAC 3′ TT8R       PstI

The TT8 PCR fragment is A-tailed and ligated into pGEMT, then excisedwith NdeI and PstI and ligated into the NdeI and PstI sites of BJ60, 5′to the uidA reporter which includes a terminator signal, forming thevector TT8-BJ60.

3a(ii) TT12

A reporter vector based on the promoter of the TT12 gene (Debeaujon etal., 2000; At3g59030, accession no. AJ294464) is constructed asdescribed below. A 1.7 kb fragment including the TT12 promoter isamplified by PCR from Arabidopsis thaliana genomic DNA 5′ totranslational start of the TT12 gene using the primers TT12F and TT12Rwhich introduce an NdeI and a PstI site at the 5′ and 3′ ends of theTT12 PCR fragment respectively.

SEQ ID NO. 13 5′ AAACATATGGGAATTCACAATCGGAAAGTC 3′ TT12F       NdeI SEQID NO. 14 5′ AAACTGCAGGGTCCGTTTATTAGTTCCTC 3′ TT12R       PstI

The TT12 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and PstI and ligated into the NdeI and PstI sites ofBJ60, 5′ to the uidA reporter gene forming TT12-BJ60.

3b Construction of Binary Vectors and Transformation into Arabidopsisthaliana

Reporter cassettes are excised with NotI from the following vectors:

-   -   TT8-BJ60    -   TT12-BJ60    -   and ligated into the NotI sites of the binary vector BJ40,        forming the following vectors for transformation:    -   TT8-uidA-BJ40    -   TT12-uidA-BJ40

The binary vectors are transformed into Agrobacterium tumefaciens andthen into Arabidopsis thaliana.

3c Analysis of Expression Patterns

The uidA gene encodes β-glucuronidase (GUS), which is assayed usingstandard protocols (e.g. Jefferson, 1987). For FIG. 12 (below) thefollowing assay was used. Seeds were dissected from siliques into GUSstaining buffer (100 mM Tris-HCl pH 7.2, 50 mM NaCl, 0.1% Triton-X-100,2 mM 5-bromo-4-chloro-3-indolyl-beta-D-glucoronic acid (X-Gluc), 2 mMK₃Fe(CN₆), 2 mM K₄Fe(CN)₆) and incubated overnight at 37° C.

FIG. 12 shows a globular stage seed from a plant containing theTT12::uidA construct assayed for GUS expression; the inner layer of theinner integument is stained (arrow), indicating activity of the TT12promoter fragment in that integument.

Example 4 Construction and Transformation of an RNAi Cassette thatDecreases MNT Expression In Arabidopsis thaliana, Including DecreasedExpression in the Integuments/Seed Coat

The cloning strategy is shown in FIG. 13A.

4a Construction of RNAi Cassette

An RNAi vector based on the MNT gene (see above) is constructed asdescribed below. A 0.57 kb fragment of the MNT cDNA (‘MNTi’) isamplified by PCR from Arabidopsis thaliana cDNA using the primers FARF2i and RARF2inew which introduce XbaI and AscI sites at the 5′ end of theMNTi PCR fragment, and BamHI and SwaI sites at the 3′ end of the PCRfragment.

SEQ ID NO. 15 5′ GATCTAGAGGCGCGCCGGATCTGAGAACTGGATG 3′ FARF2i     XbaI    AscI SEQ ID NO. 16 5′ GAGGATCCATTTAAATCCGCAGCATCATTCAAGT 3′RARF2inew      BamHI    SwaI

The MNTi PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with AscI and SwaI and ligated into the AscI and Swal sites ofthe pFGC5941 RNAi vector 3′ to the 35S promoter and 5′ to the CHSAintron, which places the fragment in forward orientation. This forms thevector 35S-MNTi-pFGC5941. The MNTi PCR fragment is then excised frompGEMT with BamHI and XbaI and ligated into the BamHI and XbaI sites ofthe 35S-MNTi-pFGC5941 vector, 3′ to the CHSA intron and 5′ to the ocsterminator signal, which places the fragment in inverse orientation.This forms the vector 35S-MNTi-inv MNTi-pFGC5941.

4b Transformation into Arabidopsis thaliana

Vector 35S-MNTi-inv MNTi-pFGC5941 is transformed into Agrobacteriumtumefaciens and then into Arabidopsis thaliana.

4c Analysis of Seed Weights in Plants Transformed with the 35S::MNT RNAiVector

Wild-type plants transformed with the 35S::MNT RNAi vector described inExample 4a, b have the mnt mutant phenotype, including closed flowersfor most of the plant's life cycle (FIG. 13B top left), inflorescencestems with increased diameter (FIG. 13B top right), and large seeds(FIG. 13B, bottom). Seeds from four independently transformed lines,along with wild-type plants grown under the same conditions, are shownin FIG. 13B (bottom). The mean weight for these four lines was 35.3 μg,compared with 13.8 μg for the wild-type control.

Example 5 Construction and Transformation of an RNAi Cassette thatDecreases BnARF2 Expression in Brassica napus, Including DecreasedExpression in the Integuments/Seed Coat

The cloning strategy is shown in FIG. 14.

5a Construction of RNAi Cassette

An RNAi vector based on the B ARF2 gene (Example 2, above) isconstructed as described below. A 0.56 kb fragment of the BnARF2 cDNA(BnARF21) is amplified by PCR from Brassica napus cDNA using the primersFBnARF2 i and RBnARF2 i which introduce XbaI and AscI sites at the 5′end of the BnARF2 i PCR fragment, and BamHI and SwaI sites at the 3′ endof the PCR fragment.

SEQ ID NO. 17 5′ GATCTAGAGGCGCGCCGCGATATGAGAACTGGATA 3′ FBnARF2i     XbaI    AscI SEQ ID NO. 18 5′ GAGGATCCATTTAAATGTAGGCCCCGCAGGGTCA 3′RBnARF2i      BamHI   SwaI

The BnARF21 PCR fragment is A-tailed and ligated into pGEMT and thenexcised with AscI and SwaI and ligated into the AscI and SwaI sites ofthe pFGC5941 RNAi vector 3′ to the 35S promoter and 5′ to the CHSAintron using the enzymes Ascl and SwaI, which places the fragment inforward orientation. This forms the vector 35S-BnARF21-pFGC5941. TheBnARF21 PCR fragment is then excised from pGEMT with BamHI and XbaI andligated into the BamHI and XbaI sites of the 35S-BnARF21-pFGC5941 vector3′ to the CHSA intron and 5′ to the ocs terminator, which places thefragment in inverse orientation. This forms the vector 35S-BnARF21-invBnARF21-pFGC5941.

5b Transformation

Vector 35S-BnARF21-inv BnARF21-pFGC5941 is transformed intoAgrobacterium tumefaciens and then into Brassica napus.

Example 6 Construction and Transformation of RNAi Cassettes thatDecrease MNT Expression Primarily in the Integuments/Seed Coat ofArabidopsis thaliana

This is specifically to phenocopy the big seed effect of mnt mutationswithout other effects on plant growth, development, or fertility.

The cloning strategy is shown in FIG. 15.

6a Construction of RNAi Vectors Containing an Integument/Seed CoatPromoter6a(i) TT8

An RNAi vector in which the TT8 promoter (Nesi et al., 2000; At4g09820,accession no. AJ277509) drives an inverted repeat of an MNT nucleic acidfragment (see Example 4, above) is constructed as described below. A 1.7kb fragment including the TT8 promoter is amplified by PCR fromArabidopsis thaliana genomic DNA 5′ to translational start of the TT8gene using the primers TT8 EcoRI F and TT8 NcoI R which introduce anEcoRI and an NcoI site at the 5′ and 3′ ends of the TT8 PCR fragmentrespectively.

SEQ ID NO. 19 5′ GAATTCCCAACGGGATCATGGGATTAC 3′ TT8Fi    EcoRI SEQ IDNO. 20 5′ CCATGGCGTTCCCGGAGATACGAAAAC 3′ TT8Ri    NcoI

The TT8 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with EcoRI and NcoI and exchanged for the 35S promoter in thevector 35S-MNT-inv M1MNTi-pFGC5941 (Example 4, above), forming thevector TT8-MNT-inv MNTi-pFGC5941.

6a(ii) INO

An RNAi vector in which the INO promoter (Villanueva et al., 1999;At1g23420, accession no. AF195047) drives an inverted repeat of an MNTnucleic acid fragment (see Example 4, above) is constructed as describedbelow. A 1.5 kb fragment including the INO promoter is amplified by PCRfrom Arabidopsis thaliana genomic DNA 5′ to translational start of theINO gene using the primers FINOi and RINOi_which introduce an EcoRI andan NcoI site at the 5′ and 3′ ends of the INO PCR fragment respectively.

SEQ ID NO. 21 5′ GAATTCCCTGGATTAGTGCAAGCC 3′ FINOi    EcoRI SEQ ID NO.22 5′ CCATGGGAGAGTGTGTGTGTACGATG 3′ RINOi    NcoI

The INO PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with EcoRI and NcoI and exchanged for the 35S promoter in thevector 35S-MNT-inv MNTi-pFGC5941 (Example 4, above), forming the vectorINO-MNT-inv MNTi-pFGC5941.

6b Transformation into Arabidopsis thaliana

The TT8-MNT-inv MNTi-pFGC5941 and INO-MNT-inv MNTi-pFGC5941 vectors aretransformed into Agrobacterium tumefaciens and then into Arabidopsisthaliana.

Example 7 Construction and Transformation of RNAi Cassettes thatDecrease BnARF2 Expression Primarily in the Integuments/Seed Coat ofBrassica napus

The cloning strategy is shown in FIG. 16.

7a Construction of RNAi Vectors Containing an Integument/Seed CoatPromoter7a(i) TT8

An RNAi vector in which the TT8 promoter (Nesi et al., 2000; At4g09820,accession no. AJ277509) drives an inverted repeat of a BnARF2 nucleicacid fragment (see Example 5, above) is constructed as described below.A 1.7 kb fragment including the TT8 promoter with EcoRI and NcoI linkersis amplified by PCR from Arabidopsis thaliana genomic DNA as describedin Example 6a(i) above.

The TT8 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with EcoRI and NcoI and exchanged for the 35S promoter in thevector 35S-BnARF2-inv BnARF21-pFGC5941 (Example 5, above), forming thevector TT8-BnARF2-inv BnARF21-pFGC5941.

7a(ii) INO

An RNAi vector in which the INO promoter (Villanueva et al., 1999;At1g23420, accession no. AF195047) drives an inverted repeat of a BnARF2nucleic acid fragment (see Example 5, above) is constructed as describedbelow. A 1.5 kb fragment including the INO promoter with EcoRI and NcoIlinkers is amplified by PCR from Arabidopsis thaliana genomic DNA asdescribed in Example 6a(ii) above.

The INO PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with EcoRI and NcoI and exchanged for the 35S promoter in thevector 35S-BnARF2-inv BnARF21-pFGC5941 (Example 5, above), forming thevector INO-BnARF2-inv BnARF21-pFGC5941.

7b Transformation into Brassica napus

The TT8-BnARF2-inv BnARF21-pFGC5941 and INO-BnARF2-inv BnARF21-pFGC5941vectors are transformed into Agrobacterium tumefaciens and then intoBrassica napus.

Example 8 Construction and Transformation of an Expression Vector thatIncreases MNT expression in Arabidopsis thaliana, including increasedexpression in the integuments/seed coat

This is to produce a plant with altered seed size.

The cloning strategy is shown in FIG. 17.

8a Construction of a Vector for Constitutive Expression of MNT

Construction of an expression vector with the CaMV 35S promoter drivingthe MNT gene is described below. The MNT cDNA including thetranslational start and stop is amplified by PCR from Arabidopsisthaliana cDNA using the primers 35S Xho new and 35S Bam new whichintroduce a XhoI and a BamHI site at the 5′ and 3′ ends of the A4NT PCRfragment respectively.

SEQ ID NO. 23 5′ CTCGAGGAAGGTATGGCGAGT 3′ 35S Xho new    XhoI SEQ ID NO.24 5′ GGATCCTCCAGTCTCCACCAA 3′ 35S Bam new    BamHI

The MNT PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with XhoI and BamHI and ligated into the XhoI and BamHI sites ofpART7, 3′ to the 35S promoter and 5′ to the ocs terminator, forming thevector 35S-MNT-pART7.

8b Construction of Binary Vectors and Transformation into Arabidopsisthaliana

The 35 S::MNT expression cassette (including the ocs terminator signal)is excised from 35S-MNT-pART7 with NotI and ligated into the NotI sitesof the binary vector BJ40, forming the vector 35S-MNT-BJ40. The binaryvector is transformed into Agrobacterium tumefaciens and then intoArabidopsis thaliana.

8c Analysis of Seed Weights in Plants Transformed with the 35S::MNTCassette

Wild-type plants transformed with the 35S::MNT cassette described inExample 8a, b have the mnt mutant phenotype, including closed flowersfor most of the plant's life cycle (FIG. 17B, top), and large seeds.Seeds from three independently transformed lines, along with wild-typeplants grown under the same conditions, are shown in FIG. 17B, middle.The overall mean weight for these three lines was 25.5 μg, compared with15.0 μg for the wild-type control. Expression of MNT/ARF2 was assayed intransformed and wild-type plants by semiquantitative RT-PCR (FIG. 17B,bottom) using multiplex RT-PCR with primers RTARF2-F(5′-GAGTGGGTGGAGTGTGTTTG-3′) and RTARF2-R (5′-AGTTGGTTTTCGTTTGAGCAT-3′),and control primers to the GAPC gene, GAPC-F(5′-CACTTGAAGGGTGGTGCCAAG-3′) and GAPC-R (5′-CCTGTTGTCGCCAACGAAGTC-3′).PCR was initiated with RTARF2 primers and run for 4 cycles at anannealing temperature of 55° C., extension time 2 min. GAPC primers wereadded to each reaction mix and the reaction was run for an additional 22cycles. This showed that plants transformed with the 35S::MNT cassettedid not have lower levels of MNT expression than wild-type plants;therefore the mutant phenotype was not due to cosuppression. Thereforeconstitutive expression of the MNT gene (such as achieved under controlof the 35S promoter) provides a further method for producing largeseeds.

Example 9 Construction and Transformation of an Expression Cassette thatIncreases BnARF2 Expression in Brassica napus, Including IncreasedExpression in the Integuments/Seed Coat

This is also to produce a plant with altered seed size.

The cloning strategy is shown in FIG. 17.

9a Construction of a Vector for Constitutive Expression of BnARF2

Construction of an expression vector with the CaMV 35S promoter drivingthe BnARF2 gene is described below. The BnARF2 cDNA from translationalstart to stop is amplified by PCR from Brassica napus cDNA using theprimers BnARF2 XhoI F and BnARF2 BamHI R which introduce a XhoI and aBamHI site at the 5′ and 3′ ends of the BnARF2 PCR fragmentrespectively.

SEQ ID NO. 25 5′ CTCGAGATGGCGAGTTCGGAGGTTTC 3′ BnARF2 XhoI F    XhoI SEQID NO. 26 5′ GGATCCTTAAGAGTTTCCGGCGCTGG 3′ BnARF2 BamHI R    BamHI

The BnARF2 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with XhoI and BamHI and ligated into the XhoI and BamHI sites ofpART7, 3′ to the 35S promoter and 5′ to the ocs terminator, forming thevector 35S-BnARF2-pART7.

9b Construction of Binary Vectors and Transformation into Brassica napus

The 35S::BnARF2 expression cassette (including the ocs terminatorsignal) is excised from 35S-BnARF2-pART7 with NotI and cloned into theNotI sites of the binary vector BJ40, forming the vector35S-BnARF2-BJ40.

The binary vector is transformed into Agrobacterium tumefaciens and theninto Brassica napus. Constitutive expression of the BnARF2 gene (such asachieved under control of the 35S promoter) provides a further methodfor producing large seeds.

Example 10 Construction and Transformation of Expression Cassettes thatIncrease MNT Expression Primarily in the Integuments/Seed Coat ofArabidopsis thaliana

The cloning strategy is shown in FIG. 18.

10a Construction of Expression Vectors Containing an Integument/SeedCoat Promoter10a(i) TT8

An expression vector based on the TT8 promoter (Nesi et al., 2000;At4g09820, accession no. AJ277509) is constructed as described below. A1.7 kb fragment including the TT8 promoter with NdeI and PstI linkers isamplified by PCR from Arabidopsis thaliana genomic DNA as described inExample 3a(i), above. The TT8 PCR fragment is A-tailed and ligated intopGEMT, and then excised with NdeI and PstI and ligated into the NdeI andPstI sites of BJ36, 5′ to the ocs terminator signal, forming the vectorTT8-BJ36.

10a(ii) INO

An expression vector based on the promoter of the INO gene (Villanuevaet al., 1999; At1g23420, accession no. AF195047) is constructed asdescribed below. A 1.5 kb fragment including the INO promoter isamplified by PCR from Arabidopsis thaliana genomic DNA 5′ totranslational start of the INO gene using the primers INOF and INORwhich introduce an NdeI and a PstI site at the 5′ and 3′ ends of the INOPCR fragment respectively.

SEQ ID NO. 27 5′ CATATGCCTGGATTAGTGCAAGGCAA 3′ INOF    NdeI SEQ ID NO.28 5′ CTGCAGGAGAGTGTGTGTGTACGATG 3′ INOR    PstI

The INO PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and PstI and ligated into the NdeI and PstI sites ofBJ36, 5′ to the ocs terminator signal, forming the vector INO-BJ36.

10b Construction of Expression Vectors Containing a Promoter::MNTExpression Cassette

The MNT cDNA with XhoI and BamHI linkers is amplified by PCR fromArabidopsis thaliana cDNA and ligated into pGEMT as described in Example8a, above.

10b(i) TT8-MNT

The MNT PCR fragment is excised from pGEMT with XhoI and BamHI andligated into the XhoI and BamHI sites of the TT8-BJ36 vector, 3′ to theTT8 promoter, forming the vector TT8-MNT-BJ36.

10 b(ii) INO-MNT

The MNT PCR fragment is excised from pGEMT with XhoI and BamHI andligated into the XhoI and BamHI sites of the INO-BJ36 vector, 3′ to theINO promoter, forming the vector INO-MNT-BJ36.

10c Construction of Binary Vectors and Transformation10c(i) TT8-MNT

The TT8::MNT expression cassette (including the ocs terminator signal)is excised from TT8-MNT-BJ36 with NotI and cloned into the NotI sites ofthe binary vector BJ40, forming the vector TT8-MNT-BJ40.

10c(ii) INO-MNT

The INO::MNT expression cassette (including the ocs terminator signal)is excised from INO-MNT-BJ36 with NotI and cloned into the NotI sites ofthe binary vector BJ40, forming the vector INO-MNT-BJ40.

The TT8-MNT-BJ40 and INO-MNT-BJ40 binary vectors are transformed intoAgrobacterium tumefaciens and then into Arabidopsis thaliana.

Example 11 Construction and Transformation of Expression Vectors thatIncrease BnARF2 Expression Primarily in the Integuments/Seed Coat ofBrassica napus

The cloning strategy is shown in FIG. 19.

11a Construction of Expression Vectors Containing an Integument/SeedCoat Promoter11a(i) TT8

An expression vector based on the promoter of the TT8 gene (Nesi et al.,2000; At4g09820, accession no. AJ277509) is constructed as describedbelow. A 1.7 kb fragment including the TT8 promoter is amplified by PCRfrom Arabidopsis thaliana genomic DNA 5′ to translational start of theTT8 gene using the primers TT8F and TT8 MluI R which introduce an NdeIand an MluI site at the 5′ and 3′ ends of the TT8 PCR fragmentrespectively.

SEQ ID NO. 11 5′ AAACATATGCCAACGGGATCATGGGATTAC 3′ TT8F       NdeI SEQID NO. 29 5′ AAAACGCGTCGTTCCCGGAGATACGAAAAC 3′ TT8 MluI R       MluI

The TT8 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and MluI and ligated into the NdeI and MluI sites ofBJ36, 5′ to the ocs terminator signal, forming the vector TT8 (NdeIMluI)-BJ36.

11 a(ii) INO

An expression vector based on the promoter of the INO gene (Villanuevaet al., 1999; At1g23420, accession no. AF195047) is constructed asdescribed below. A 1.5 kb fragment including the INO promoter isamplified by PCR from Arabidopsis thaliana genomic DNA 5′ totranslational start of the INO gene using the primers INOF and INO MluIR which introduce an NdeI and an MluI site at the 5′ and 3′ ends of theINO PCR fragment respectively.

SEQ ID NO. 27 5′ CATATGCCTGGATTAGTGCAAGGCAA 3′ INOF    NdeI SEQ ID NO.30 5′ ACGCGTGAGAGTGTGTGTCTACGATG 3′ INO MluI R    MluI

The INO PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and MluI and ligated into the NdeI and MluI sites ofBJ36, 5′ to the ocs terminator signal, forming the vector INO (NdeIMluI)-BJ36.

11b Construction of Expression Vectors Containing a Promoter::BnARF2Expression Cassette

The BnARF2 cDNA with XhoI and BamHI linkers is amplified by PCR fromBrassica napus cDNA and ligated into pGEMT as described in Example 9a,above.

11 b(i) TT8

The BnARF2 PCR fragment is excised from pGEMT with XhoI and BamHI andligated into the XhoI and BamHI sites of the TT8 (NdeI MluI)-BJ36vector, 3′ to the TT8 promoter, forming the vector TT8-BnARF2-BJ36.

11b(ii) INO

The BnARF2 PCR fragment is excised from pGEMT with XhoI and BamHI andligated into the XhoI and BamHI sites of the INO (NdeI MluI)-BJ36vector, 3′ to the INO promoter, forming the vector INO-BnARF2-BJ36.

11c Construction of Binary Vectors and Transformation

11c(i) TT8

The TT8-BnARF2 expression cassette (including the ocs terminator signal)is excised from TT8-BnARF2-BJ36 with NotI and ligated into the NotIsites of the binary vector BJ40, forming the vector TT8-BnARF2-BJ40.

11c(ii) INO

The INO-BnARF2 expression cassette (including the ocs terminator signal)is excised from INO-BnARF2-BJ36 with NotI and ligated into the NotIsites of the binary vector BJ40, forming the vector INO-BnARF2-BJ40.

The binary vectors TT8-BnARF2-BJ40 and INO-BnARF2-BJ40 are transformedinto Agrobacterium tumefaciens and then into Brassica napus.

Example 12 Construction, Transformation, and Analysis of ExpressionVectors that Increase Expression of a Gene Promoting Cell Division inthe Integuments/Seed Coat of Arabidopsis thaliana

The cloning strategy is shown in FIG. 20.

12a Construction of expression vectors containing an integument/seedcoat promoter

12a(i) TT8

An expression vector based on the TT8 promoter (Nesi et al., 2000;At4g09820, accession no. AJ277509) is constructed as described below. A1.7 kb fragment including the TT8 promoter with NdeI and PstI linkers isamplified by PCR from Arabidopsis thaliana genomic DNA as described inExample 3a(i), above. The TT8 PCR fragment is A-tailed and ligated intopGEMT, and then excised with NdeI and PstI and ligated into the NdeI andPstI sites of BJ36, 5′ to the ocs terminator signal, forming the vectorTT8-BJ36.

12a(ii) TT12

An expression vector based on the TT12 promoter (Debeaujon et al., 2000;At3g59030, accession no. AJ294464) is constructed as described below. A1.7 kb fragment including the TT12 promoter with NdeI and PstI linkersis amplified by PCR from Arabidopsis thaliana genomic DNA as describedin Example 3a(ii), above. The TT12 PCR fragment is A-tailed and ligatedinto pGEMT, and then excised with NdeI and PstI and ligated into theNdeI and PstI sites of BJ36, 5′ to the ocs terminator signal, formingthe vector TT12-BJ36.

12a(iii) INO

An expression vector based on the INO promoter (Villanueva et al., 1999;At1g23420, accession no. AF195047) is constructed as described below. A1.5 kb fragment including the INO promoter with NdeI and PstI linkers isamplified by PCR from Arabidopsis thaliana genomic DNA as described inExample 10a(ii), above. The INO PCR fragment is A-tailed and ligatedinto pGEMT, and then excised with NdeI and PstI and ligated into theNdeI and PstI sites of BJ36, 5′ to the ocs terminator signal, formingthe vector INO-BJ36.

12a(iv) BAN

An expression vector based on the promoter of the BAN gene (Devic etal., 1999; At1g61720, accession no. AF092912) is constructed asdescribed below. A 0.4 kb fragment including the BAN promoter isamplified by PCR from Arabidopsis thaliana genomic DNA 5′ totranslational start of the BAN gene using the primers BANF and BANRwhich introduce an NdeI and a PstI site at the 5′ and 3′ ends of the BANPCR fragment respectively.

SEQ ID NO. 31 5′ CATATGGAGAATTTGACAGATTGGTG 3′ BANF    NdeI SEQ ID NO.32 5′ CTGCAGGTTTATCGTCTTGAGACTTC 3′ BANR    PstI

The BAN PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and PstI and ligated into the NdeI and PstI sites ofBJ36, 5′ to the ocs terminator signal, forming the vector BAN-BJ36.

12b Construction of Expression Cassettes Containing are Integument/SeedCoat Promoter Driving a Gene Promoting Cell Division12b(i) Promoter::CYCD3;1

Construction of expression vectors with an integument seed coat promoterdriving the CYCD3;1 gene is described below. The CYCD3;1 cDNA (formerlyCycδ3; Soni et al., 1995; Vandepoele et al., 2002; At4g34160, accessionno. X83371) is amplified by PCR from Arabidopsis thaliana cDNA using theprimers CYCD3F and CYCD3R which introduce a SmaI and a BamHI site at the5′ and 3′ ends of the CYCD3;1 PCR fragment respectively.

SEQ ID NO. 33 5′ AAACCCGGGATGGCGATTCGGAAGGAGGAA 3′ CYCD3F       SmaI SEQID NO. 34 5′ AAAGGATCCTTATGGAGTGGCTACGATTGC 3′ CYCD3R       BamHI

The CYCD3;1 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with SmaI and BamHI and ligated into the SmaI and BamHI sites ofthe following vectors:

TT8-BJ36 vector, 3′ to the TT8 promoter and 5′ to the ocs terminatorsignal, forming the vector TT8-CYCD3;1-BJ36 TT12-BJ36 vector, 3′ to theTT12 promoter and 5′ to the ocs terminator signal, forming the vectorTT12-CYCD3;1-BJ36 INO-BJ36 vector, 3′ to the INO promoter and 5′ to theocs terminator signal, forming the vector INO-CYCD3;1-BJ36 BAN-BJ36vector, 3′ to the BAN promoter and 5′ to the ocs terminator signal,forming the vector BAN-CYCD3;1-BJ36

12b(ii) Promoter::IPT1

Construction of expression vectors with an integument/seed coat promoterdriving the IPT1 gene is described below. The IPT1 gene (Takei et al.,2001; At1g68460, accession no. AB062607) is amplified by PCR fromArabidopsis thaliana genomic DNA (the IPT1 gene contains no introns)using the primers IPT1F and IPT1R which introduce a SmaI and a BamHIsite at the 5′ and 3′ ends of the IPT1 PCR fragment respectively.

SEQ ID NO. 35 5′ AAACCCGGGATGACAGAACTCAACTTCCAC 3′ IPT1F       SmaI SEQID NO. 36 5′ AAAGGATCCCTAATTTTGCACCAAATGCCG 3′ IPT1R       BamHI

The IPT1PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with SmaI and BamHI and ligated into the SmaI and BamHI sites ofthe following vectors:

TT8-BJ36 vector, 3′ to the TT8 promoter and 5′ to the ocs terminatorsignal, forming the vector TT8-IPT1-BJ36 TT12-BJ36 vector, 3′ to theTT12 promoter and 5′ to the ocs terminator signal, forming the vectorTT12-IPT1-BJ36 INO-BJ36 vector, 3′ to the INO promoter and 5′ to the ocsterminator signal, forming the vector INO-IPT 1-BJ36 BAN-BJ36 vector, 3′to the BAN promoter and 5′ to the ocs terminator signal, forming thevector BAN-IPT1-BJ36

12b(iii) Promoter::ANT

Construction of expression vectors with an integument/seed coat promoterdriving the ANT gene is described below. The ANT gene (Klucher et al.,1996; At4g37750, accession no. NM_(—)119937) is amplified by PCR fromArabidopsis thaliana cDNA using the primers ANTF and ANTR whichintroduce a SmaI and a BamHI site at the 5′ and 3′ ends of the ANT PCRfragment respectively.

SEQ ID NO. 37 5′ CCCGGGGGTGTGTTCGTTGTGTAACC 3′ ANTF    SmaI SEQ ID NO.38 5′ GGATCCGATCAAGAATCAGCCCAAGC 3′ ANTR    BamHI

The ANT PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with SmaI and BamHI and ligated into the SmaI and BamHI sites ofthe following vectors:

TT8-BJ36 vector, 3′ to the TT8 promoter and 5′ to the ocs terminatorsignal, forming the vector TT8-ANT-BJ36 TT12-BJ36 vector, 3′ to the TT12promoter and 5′ to the ocs terminator signal, forming the vectorTT12-ANT-BJ36 INO-BJ36 vector, 3′ to the INO promoter and 5′ to the ocsterminator signal, forming the vector INO-ANT-BJ36 BAN-BJ36 vector, 3′to the BAN promoter and 5′ to the ocs terminator signal, forming thevector BAN-ANT-BJ36

12b(iv) Promoter:: CYCB1;1

Construction of expression vectors with an integument/seed coat promoterdriving the CYCB1;1 gene is described below. The CYCB1;1 gene (formerlyCyc1aAt; Ferreira et al., 1994; Vandepoele et al., 2002; At4g37490,accession no. NM_(—)119913) is amplified by PCR from Arabidopsisthaliana cDNA using the primers CYCB1F and CYCB1R which introduce a SmaIand a BamHI site at the 5′ and 3′ ends of the CYCB1;1 PCR fragmentrespectively.

SEQ ID NO. 39 5′ CCCGGGCACTAAGATGATGACTTCTC 3′ CB1F    SmaI SEQ ID NO.40 5′ GGATCCAAGCGACTCATTAGACTTGT 3′ CB1R    BamHI

The CYCB1;1 PCR fragment is A-tailed and ligated into pGEMT, and thereexcised with SmaI and BamHI and ligated into the SmaI and BamHI sites ofthe following vectors:

TT8-BJ36 vector, 3′ to the TT8 promoter and 5′ to the ocs terminatorsignal, forming the vector TT8-CYCB1;1-BJ36

TT12-BJ36 vector, 3′ to the TT12 promoter and 5′ to the ocs terminatorsignal, forming the vector TT12-CYCB1;1-BJ36 INO-BJ36 vector, 3′ to theINO promoter and 5′ to the ocs terminator signal, forming the vectorINO-CYCB1;1-BJ36 BAN-BJ36 vector, 3′ to the BAN promoter and 5′ to theocs terminator signal, forming the vector BAN-CYCB1;1-BJ36

12c Construction of Binary Vectors and Transformation into Arabidopsisthaliana

Expression cassettes (including the ocs terminator) are excised withNotI from the following vectors

TT8-CYCD3;1-BJ36 TT8-IPT1-BJ36 TT8-ANT-BJ36 TT8-CYCB1;1-BJ36TT12-CYCD3;1-BJ36 TT12-IPT1-BJ36 TT12-ANT-BJ36 TT12-CYCB1;1-BJ36INO-CYCD3;1-BJ36 INO-IPT1-BJ36 INO-ANT-BJ36 INO-CYCB1;1-BJ36BAN-CYCD3;1-BJ36 BAN-IPT1-BJ36 BAN-ANT-BJ36 BAN-CYCB1;1-BJ36

and ligated into the NotI sites of the binary vector BJ40, forming thefollowing vectors for transformation:

TT8-CYCD3;1-BJ40 TT8-IPT1-BJ40 TT8-ANT-BJ40 TT8-CYCB1;1-BJ40TT12-CYCD3;1-BJ40 TT12-IPT1-BJ40 TT12-ANT-BJ40 TT12-CYCB1;1-BJ40INO-CYCD3;1-BJ40 INO-IPT1-BJ40 INO-ANT-BJ40 INO-CYCB1;1-BJ40BAN-CYCD3;1-BJ40 BAN-IPT1-BJ40 BAN-ANT-BJ40

BAN-CYCB1;1-BJ40

The binary vectors are transformed into Agrobacterium tumefaciens andthen into Arabidopsis thaliana.

12d Analysis of Seed Weights in Transformants

Results from some primary transformants using the TT8 promoter are shownin Table 2A and FIG. 21A. The histogram shows that seeds fromTT8::CYCD3;1 and TT8::IPT1 plants have a broader distribution and higherpeak of weights than the controls. TT8::uidA lines were used ascontrols, as expression of the uidA gene is not found to affect plantgrowth and development. Individual TT8::CYCD3;1 plants produced seeds upto 97% heavier than controls, with a mean increase over 27 lines of 37%.TT8::IPT1 plants produced seeds up to 107% heavier, with a mean increaseover 24 lines of 28%. The mean weights of TT8::CYCD3;1 and TT8::IPT1seeds were compared with the controls using t-tests and found to besignificantly different from the controls with P<0.000. It should benoted that some of the TT8::IPT1 lines, including the highest weighingline, also had a vegetative phenotype including dwarfing, serratedleaves, and extremely low fertility, most likely due to the TT8 promoterdriving vegetative expression of IPT1 in some lines. However lines withnormal vegetative development also produced large seeds. It is likelythat vegetative expression of TT8 could be prevented if required by thetechnique of promoter dissection (e.g. Chandrasekharan et al., 2003).

TABLE 2A Seed weights in individual primary transformants from TT8::GUS(control), TT8::CYCD3;1, and TT8::IPT1 families TT8::GUS (controls)TT8::CYCD3;1 TT8:IPT1 17.0 μg (n = 52) 19.0 μg (n = 77) 21.8 μg (n = 45)14.2 (79) 21.6 (61) 15.6 (62) 14.7 (51) 22.5 (52) 23.4 (68) 13.9 (47)17.9 (52) 20.9 (95) 14.7 (66) 17.5 (63) 11.2 (58) 15.1 (43) 16.9 (89)19.3 (89) 14.2 (50) 16.6 (54) *19.9 (119) 14.8 (61) 18.6 (57) 17.9 (64)13.9 (54) 17.7 (56) 24.3 (64) 18.6 (54) 21.9 (57) 13.2 (48) 29.2 (49)17.6 (72) 18.2 (49) 20.8 (66) 17.0 (72) *30.6 (43)  23.0 (45) 14.0 (61)18.6 (56) 19.5 (64) 28.1 (56) 20.5 (47) 20.1 (47) 18.8 (68) 17.8 (47)15.8 (65) 18.8 (58) 22.1 (47) 26.1 (55) 14.2 (47) 16.4 (55) 19.6 (49)24.6 (56) 17.3 (50) 19.5 (49) *26.7 (51)  16.1 (51) 25.8 (58) 18.0 (62)*plants with very low fertility Mean 14.8 20.3 19.0 Range 13.9 to 17.013.9 to 29.2 11.2 to 30.6 Standard error  0.3  0.8  0.9 ttest forcontrol vs TT8::CYCD3;1 and TT8:IPT1, P < 0.000, significant

Further results from plants transformed with expression vectors toincrease seed size are shown in Table 2B and FIG. 21B. For theseexperiments, we selected kanamycin resistant lines with heavy seeds andconfirmed the presence of the expression vector using PCR. For two ofthe lines below we weighed seeds produced by T3 plants, confirming theheritability of the large seed trait. In Table 2B, weights of controls(in this case the controls were wild-type Col-0 are shown alongsidetransformants where the controls and transformants were grown together.BAN::CYCD3;1 seeds were 35% heavier than controls grown under the sameconditions, and INO::ANT seeds were 53% heavier. INO::ANT seeds werealso misshapen (FIG. 21B), suggesting that the expression cassetteindeed affects seed coat development.

TABLE 2B Seed weights from plants transformed with expression cassettesto increase seed size transformant w.t. Col-3 (controls) BAN::CYCD3;123.9 μg 17.7 μg (seeds from T2 plants) INO::ANT (T2) 23.1 15.1 INO::IPT1(T3) 26.4 TT8::CYCD3;1 (T3) 23.2

Example 13 Construction, Transformation, and Analysis of ExpressionVectors that Increase Expression of a Gene Promoting Cell Division inthe Integuments/Seed Coat of Brassica napus

The binary vectors described in Example 12c (above) are transformed intoBrassica napus.

Example 14 Construction of an Expression Vector Containing a Petal- andStamen-Specific Promoter Driving MNT and Transformation into MNT Mutants

The cloning strategy is shown in FIG. 22.

14a Construction of an Expression Vector Based on the AP3 Promoter

An expression vector based on the promoter of the AP3 gene (Jack et al.,1992; At3g54340, accession no. AY142590) is constructed as describedbelow. A 1 kb fragment including the AP3 promoter is amplified by PCRfrom Arabidopsis thaliana genomic DNA 5′ to translational start of theAP3 gene using the primers AP3F and AP3R which introduce an NdeI and aPstI site at the 5′ and 3′ ends of the AP3 PCR fragment respectively.

SEQ ID NO. 41 5′ AAACATATGGATACACAAGTTCTTTGG 3′ AP3F       NdeI SEQ IDNO. 42 5′ AAACTGCAGATTCTTCTCTCTTTGTTTAA 3′ AP3R       PstI

The AP3 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and PstI and ligated into the NdeI and PstI sites ofthe BJ36 vector, 5′ to the ocs terminator signal, forming the vectorAP3-BJ36.

14b Construction of an Expression Vector Containing an AP3::MNTExpression Cassette

The MNT cDNA with XhoI and BamHI linkers is amplified by PCR fromArabidopsis thaliana cDNA and ligated into pGEMT as described in Example8a, above. The M1T PCR fragment is excised with XhoI and BamHI andligated into the XhoI and BamHI sites of the AP3-BJ36 vector, 3′ to theAP3 promoter and 5′ to the ocs terminator, forming the vectorAP3-MNT-BJ36.

14c Construction of Binary Vector and Transformation into Arabidopsisthaliana

The AP3::MNT expression cassette (including the ocs terminator signal)is excised from AP3-MNT-BJ36 with NotI and cloned into the NotI sites ofthe binary vector BJ40, forming the vector AP3-MNT-BJ40.

The binary vector is transformed into Agrobacterium tumefaciens and theninto Arabidopsis thaliana.

Example 15 Construction of an Expression Vector Containing a Sepal- andPetal-Specific Promoter Driving MNT and Transformation Into mnt Mutants

The cloning strategy is shown in FIG. 23.

15a Construction of an Expression Vector Based on the AP1 Promoter

An expression vector based on the promoter of the AP1 gene (Mandel etal., 1992; At1g69120, accession no. NM_(—)105581) is constructed asdescribed below. A 1.7 kb fragment including the AP1 promoter isamplified by PCR from Arabidopsis thaliana genomic DNA 5′ totranslational start of the AP1 gene using the primers AP1F and AP1Rwhich introduce an NdeI and a PstI site at the 5′ and 3′ ends of the AP3PCR fragment respectively.

SEQ ID NO. 43 5′ CATATG GTGACATCTTTTTAGCATAGGTTC 3′ AP1F       NdeI SEQID NO. 44 5′ CTGCAG TTTTGATCCTTTTTTAAGAAACTT 3′ AP1R       PstI

The AP1 PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and PstI and ligated into the NdeI and PstI sites ofthe BJ36 vector, 5′ to the ocs terminator signal, forming the vectorAP1-BJ36.

15b Construction of an Expression Vector Containing an Ap1::MNTExpression Cassette

The MNT cDNA with XhoI and BamHI linkers is amplified by PCR fromArabidopsis thaliana cDNA and ligated into pGEMT as described in Example8a, above. The MNT PCR fragment is excised with XhoI and BamHI andligated into the XhoI and BamHI sites of the AP1-BJ36 vector, 3′ to theAP1 promoter and 5′ to the ocs terminator, forming the vectorAP1-MNT-BJ36.

15c Construction of Binary Vector and Transformation into Arabidopsisthaliana

The AP1::MNT expression cassette (including the ocs terminator signal)is excised from AP1-MNT-BJ36 with NotI and cloned into the NotI sites ofthe binary vector BJ40, forming the vector AP1-MNT-BJ40.

The binary vector is transformed into Agrobacterium tumefaciens and theninto Arabidopsis thaliana.

Example 16 Value of mnt Mutants in Understanding and Modifying Growth ofthe Inflorescence Stem

mnt-1 mutants have thick inflorescence stems compared with wild-typeplants. The increased diameter of mnt-1 stems is caused by extra celldivisions (FIG. 24B). Therefore it is expected that stem thickness maybe increased in other species by altering expression of an MNTorthologue and thereby increasing the number of cells in the stem.

Example 17 Construction and Transformation of an RNAi Cassette thatDecreases MNT Expression In Arabidopsis thaliana, Including DecreasedExpression in the Stem

The cloning and transformation strategy is described in Example 4. Thecloning strategy is shown in FIG. 13A. Transformed plants have anincreased stem diameter with respect to wild type (mean inflorescencestem diameter between nodes 2 and 3: w.t., 1.293±s.e.m. 0.4 mm, n=13;35S::MNT RNAi, 1.419±0.4, n=14; two-tailed t-test shows that diametersof w.t. and 35S::MNT RNAi stems are significantly different at P<0.05).The stem phenotype of transformed plants compared with wild-type plantsis shown in FIG. 13B.

Example 18 Construction of an Expression Vector Containing aFlower-Preferred Promoter Driving MNT and Transformation into MNTMutants

The cloning strategy is shown in FIG. 25.

18a Construction of an Expression Vector Based on the LFY Promoter

An expression vector based on the promoter of the LFY gene (Weigel etal., 1992; At5g61850, accession no. NM_(—)125579) is constructed asdescribed below. A 2.1 kb fragment including the LFY promoter isamplified by PCR from Arabidopsis thaliana genomic DNA 5′ totranslational start of the LFY gene using the primers LFYF and LFYRwhich introduce an NdeI and a PstI site at the 5′ and 3′ ends of the AP3PCR fragment respectively.

SEQ ID NO. 45 5′ CATATG TGTAACTGCAAAGTGTAGTTCGG 3′ LFYF       NdeI SEQID NO. 46 5′ CTGCAG AATCTATTTTTCTCTCTCTCTC 3′ LFYR       PstI

The LFY PCR fragment is A-tailed and ligated into pGEMT, and thenexcised with NdeI and PstI and ligated into the NdeI and PstI sites ofthe BJ36 vector, 5′ to the ocs terminator signal, forming the vectorLFY-BJ36.

18b Construction of an Expression Vector Containing an LFY::MNTExpression Cassette

The MNT cDNA with XhoI and BamHI linkers is amplified by PCR fromArabidopsis thaliana cDNA and ligated into pGEMT as described in Example8a, above. The MNT PCR fragment is excised with XhoI and BamHI andligated into the XhoI and BamHI sites of the LFY-BJ36 vector, 3′ to theLFY promoter and 5′ to the ocs terminator, forming the vectorAP1-LFY-BJ36.

18c Construction of Binary Vector and Transformation into Arabidopsisthaliana

The LFY::MNT expression cassette (including the ocs terminator signal)is excised from AP1-LFY-BJ36 with NotI and cloned into the NotI sites ofthe binary vector BJ40, forming the vector AP1-LFY-BJ40. The binaryvector is transformed into Agrobacterium tumefaciens and then intoArabidopsis thaliana.

SEQ ID NOS

1 MNT genomic DNA w.t Col-0

2 MNT cDNA w.t.Col-0

3 MNT predicted protein w.t. Col-0

4 mnt-1 genomic DNA Col-3

5 mnt-1 cDNA Col-3, translational start to stop

6 mnt-1 predicted protein Col-3

7 F primer for amplifying Brassica napus ARF2 cDNA

8 R primer for amplifying Brassica napus ARF2 cDNA

9 BnARF2 cDNA, translational start to stop

10 BnARF2 predicted protein

11 F primer for TT8 promoter with NdeI linker

12 R primer for TT8 promoter with PstI linker

13 F primer for TT12 promoter with NdeI linker

14 R primer for TT12 promoter with PstI linker

15 F primer for MNT RNAi fragment with Xbal and AscI linkers

16 R primer for MNT RNAi fragment with BamHI and SawI linkers

17 F primer for BnARF2 RNAi fragment with XbaI and AscI linkers

18 R primer for BnARF2 RNAi fragment with BamHI and SwaI linkers

19 F primer for TT8 promoter with EcoRI linker

20 R primer for TT8 promoter with NcoI linker

21 F primer for INO promoter with EcoRI linker

22 R primer for INO promoter with NcoI linker

23 F primer for ANT cDNA with XhoI linker

24 R primer for MNT cDNA with BamHI linker

25 F primer for BnARF2 cDNA with XhoI linker

26 R primer for BnARF2 cDNA with BamHI linker

27 F primer for INO promoter with NdeI linker

28 R primer for INO promoter with PstI linker

29 R primer for TT8 promoter with MluI linker

30 R primer for INO promoter with MluI linker

31 F primer for BAN promoter with NdeI linker

32 R primer for BAN promoter with PstI linker

33 F primer for CYCD3;1 cDNA with SmaI linker

34 R primer for CYCD3;1 cDNA with BamHI linker

35 F primer for IPT1 cDNA with SmaI linker

36 R primer for IPT1cDNA with BamHI linker

37 F primer for ANT cDNA with SmaI linker

38 R primer for ANT cDNA with BamHI linker

39 F primer for CYCB1;1 cDNA with SmaI linker

40 R primer for CYCB1;1 cDNA with BamHI linker

41 F primer for AP3 promoter with NdeI linker

42 R primer for AP3 promoter with PstI linker

43 F primer for AP1 promoter with NdeI linker

44 R primer for AP1 promoter with PstI linker

45 F primer for LFY promoter with NdeI linker

46 R primer for LFY promoter with PstI linker

SEQ ID NO. 1 MNT wild-type genomic DNA, Col-0agccattttgtaactgaccaccgagtaatctgtaatctgagctcttttattaatcggattgaataaattcgcttggagtccgtcagtcgtgtccgtgagcgcgtgtctcactcgcttgagctgatgaagtgcgataatgacgtggcatgttgggatggagaccaaagaccagcattttattttattttatagtaactaattttaaaaaccaaacaacctgagattaaaattttaatttttactgtactgtagtaaatttgggtcctgattaagattaggcatatttatctcatagtttataacaagtagcagctgaaatttgtattactagcttatagtaattaaactaaaaactacgttccaggttttaaattattgtttaaagaagatataataatatattaagaaaatagttaattaaggtaaggaggaaagtagggtttggtctgtaggttagggttcaaagagggaagagattaggagaaaggaagcatgaaggcatgacccatttcttcaattagtgctccttaatctggtgacacgtgtaggtcccacgtgtaatcacttcacattgttatttttcaaaaaatcaattagtaaaaacaaaactttgtccatcatcaaatagtagtagttttttatgtgtggttacaatattgtaagaagctctcccccttttactatgtaattcaaccccactctaatttttaaaatatttatgtaaagctttacccgaaaacaatctatcatgggttggtaatgacacatttcattaacagtgttagagaatgattcctttaatttttctacagtaaaatgttaggtgatctcattgtactacatcggaaaatactcaaaattatgtcgtgtaatttagataatggacgaatatggttttgaaatatttatggatacccaacaagatttcttaactagaaagacaaaaaaatagagcacattttgctcgttttccatcaaccctatttctccaatttgttcacatcatgatcaaaaatacagtagcaattaaaaaataaaataacaaatataaatggctatatagatcaaccctatctagctattagtattactagaaattgacaataaaggaaacattcacggtgtgtgagcatgtactactctacacacatgtccacagttattatatactgagtactagtatacgttgatgttatcaataataaaaactcgaaattaacaattataggtctatcactatgtatatgtccgaataatggtctaaaattgttaatataaaatacagattttatttcagctaaagatagttgaaattacacaagaaaatagaagagataaaaatgatcaatcagctatgtaagacgtcgtatggatagttcaataattgtggtaatacttaaagacatatatcaaaattatcaacaagcctcgaacacaaactttacaaaaagcctgtgtctactttatgagtgtttgattattaaattgcaaggtcgtagtataaaaatttcgtaggctttcaggacacaagattaaattcatttatctaaatggtgatggagtacttttatttttatatatcaaaatggtgatgatatacgaagaccatatatttagattattaaagaaaaaacgagaaaagaagaaagaaaatataaaaaaatggtttttctttttaacggacaaagattcctacaatggttgcttttagaccacacacaaatgctacacagtactcttgggtcccacacctcttagcaagtgcgttaccaacacgtgaatttcctctccccattttctcgtccttttcctctcaatattgtatcgtctcgttttccttgtcatatcgcgtgtgacgtgttattggcttattgctggagatagtttacgtgttgttaaaaataatttgtgcaaaatagtgtgcgtgtgttaaatattaaacgatatataataattagaagaaaataaaaagttttgtcgcgattagttatttgatatttaccttgttcttttgtttatcgctgcgacaagcaccgacggtataaaatataaagaaaaaaagaaagagagatgaaggtgagatgaatgaaagagtcgcagcgacagatctgaagagataggagaaagggaatttgagacgctgaaaaaccagcgtctacggaatggccgaattacagtcgatgcggcagagatgaaaaaaatgagaaatgaaagtgaaaaagagatgagaactttttttgggtcgcaggtagctgacgcagcaatcaacaaaagaacatggccaacgttttagtagatactactataaaagaaaaaggttgatttaattcattcgtaatttggacttaatttttttttaggaacactaattaatcttatttgccagctgtatgagtggactacaataaactcttgtctataaaccagattttcttcctttttaacgcttccacttacaacaatatatgtaaatatgtaattatgacggggcatacggaaatttaatttttgaagcagattcatcccattagccagctgtattaagtggtaatccaagagttaatttagttgttcagcaaatgattttagataaaatcaactactagtttaaaataactatcgaatgactgttaaggcttcgtattttttgttctgccatcaggatatcataaatatggttgaggttcgtataatattcgacgatcttttatatatctgagttgtaattgaattagagaaaataaaaaacagataatgaaacgtctttgtttttccataaaaagaaaaacagggtaaattaaagtacgagagattcacgagacgaaaattcctagaggcgcacgatagccaaaagaccatagaaaatgacatccgaaatatctttaaaatgctaaaatgcacatatttttctggtgccacgtagcatttttctccctctctcgttctctctacgtccacccagacctgcctgttcacagcacgacaaagccacttcccaataaaaacacaacacctttcccattgacgctctctttcccaaacaccgttatcctctttacccaatcaaaagttgacgcttgctcacgacttgttgacgccgttagtcccatctaaaaaagtaaagcagcctttcttacttgctaatcccctctacacatttaatttattttctcccctaatggattttttttggcaacttgagtatttatttttcaactcacagtaactgtaaataaataaaagtattcaactcacagtcaccagtaaataaatactaccagaccatagttttttcaagaattgttttggtcaacaattttaggatgacttaaattgctatatttctggggaaatacgacttggaaatgtctgcaatttgggtcttttcttcaatttatcttctccaatttgttttttaaaaaattaaatttagaaaaggatatgtcaattttttctattgaaaaggctttattaaaaaataagaaaaagtggaggaaagaaaataaaatcgtcacttgtctttggttttgtgaggtcgcagaccctggtcccccggaaatggttacaaccggtaatagccggtatgaaagagggaatggtaaccggtgaatgccggttatccatatgggttagaagtttaccgcggttgaaatgattgaagctgagttttgactacctctggttaagcccattggtcgcctcatacccagaaaaacaaaaggataggaaagacgaagaaataaaaagagagagaatgttagagagacaaactctgagagacaaaacaagagaaaatcgctcgtcgtcggtattcaagcgtctgtgactccgataaagcctagactagcgaggacggcgagagagagagagagagagctttggagttgtcgtatctctaaatcggaggcaatttgaggtgaaattggtggttttatcgtttgattctagggtttatcttctctgatagttttatcgagtaatgtcaaggagctaaactagtggtgattgtgtttgttagtgagataaagacaaaggaaggaatcaagtggactaccgaagcgagttttgagcttttcagagacggatttggagatttcttgttgatatcgtctgcttagaggcttatttggtaccagatgaaacagatctgagcttcggaaggtATGGCGAGTTCGGAGGTTTCAATGAAAGGTAATCGTGGAGGAGATAACTTCTCCTCCTCTGGTTTTAGTGACCCTAAGGAGACTAGAAATGTCTCCGTCGCCGGCGAGGGGCAAAAAAGTAATTCTACCCGATCCGCTGCGGCTGAGCGTGCTTgtaagtctccgtttcttagggtttcttaagcttggttttggttacagactgacttgatctaatttatcttcttcttcttcgtcttcatagTGGACCCTGAGGCTGCTCTTTACAGAGAGCTATGGCACGCTTGTGCTGGTCCGCTTGTGACGGTTCCTAGACAAGACGACCGAGTCTTCTATTTTCCTCAAGGACACATCGAGCAGgtgagatatttcatctatgagttcttgctatttttggctaaatctttgagttaacccctctgtgattcgtacctgttgagatattttctaatgaactttgtcggtttccattgttttatgattagGTGGAGGCTTCGACGAACCAGGCGGCAGAACAACAGATGCCTCTCTATGATCTTCCGTCAAAGCTTCTCTGTCGAGTTATTAATGTAGATTTAAAGgtaggtttctttaacttcttggaaaattttggtttctgtgtcttggattgtcagctaacaagagttttgtttatgattttacagGCAGAGGCAGATACAGATGAAGTTTATGCGCAGATTACTCTTCTTCCTGAGGCTAATgtaagttttgttttctgatttattggtttgagtgttgtagaggtgatcttattcttcaagatgctgaattctatatattttttgttccatacagCAAGACGAGAATGCAATTGAGAAAGAAGCGCCTCTTCCTCCACCTCCGAGGTTCCAGGTGCATTCGTTCTGCAAAACCTTGACTGCATCCGACACAAGTACACATGGTGGATTTTCTGTTCTTAGGCGACATGCGGATGAATGTCTCCCACCTCTGgttggtgtttcatttgcgcttctaactatctattcattggcttatttttcctgaattttgttctaagattgccttcaattcattttttgtttcttccctcagGATATGTCTCGACAGCCTCCCACTCAAGAGTTAGTTGCAAAGGATTTGCATGCAAATGAGTGGCGATTCAGACATATATTCCGGGgtataggaatctgtaacttttttattttctgtttttctcgagtctgtgtgtcatcaaacttatctggttgttgatgtttgtgataatggaccagGTCAACCACGGAGGCATTTGCTACAGAGTGGGTGGAGTGTGTTTGTTAGCTCCAAAAGGCTAGTTGCAGGCGATGCGTTTATATTTCTAAGgttgtggattagttcattgttttctttagctgtatctgttagtttctataatgtggaatatcttaatcttctacagGGGCGAGAATGGAGAATTAAGAGTTGGTGTAAGGCGTGCGATGCGACAACAAGGAAACGTGCCGTCTTCTGTTATATCTAGCCATAGCATGCATCTTGGAGTACTGGCCACCGCATGGCATGCCATTTCAACAGGGACTATGTTTACAGTCTACTACAAACCCAGgtttgtatttgtattagctcacaaaacagctttcagtgagctctttgctttgtatgtctctatatgtctgatgcttggtagtgaatcactctactaaattttcatgcggtgttgttttgtttaatacagGACGAGCCCATCTGAGTTTATTGTTCCGTTCGATCAGTATATGGAGTCTGTTAAGAATAACTACTCTATTGGCATGAGATTCAAAATGAGATTTGAAGGCGAAGAGGCTCCTGAGCAGAGgtaaaacctgtcttctgcttttgaaatatgttagctcttgagcctttttctcttggaataacgaacctaacaagttgtattgatttatattagGTTTACTGGCACAATCGTTGGGATTGAAGAGTCTGATCCTACTAGGTGGCCAAAATCAAAGTGGAGATCCCTCAAGgtatgacctagtttctagagaggatcaagactattgtttgaatataatgaatgctgattgttcaattgtctttcagGTGAGATGGGATGAGACTTCTAGTATTCCTCGACCTGATAGAGTATCTCCGTGGAAAGTAGAGCCAGCTCTTGCTCCTCCTGCTTTGAGTCCTGTTCCAATGCCTAGGCCTAAGAGGCCCAGATCAAATATAGCACCTTCATCTCCTGACTCTTCGATGCTTACCAGAGAAGgtaatgtcttccccttccactgtagtacacatagtagtgcgtctgaaacttaattgaacttgtcagtgggagtctaattcattgtacacaaaacagGTACAACTAAGGCAAACATGGACCCTTTACCAGCAAGCGGACTTTCAAGGGTCTTGCAAGGTCAAGAATACTCGACCTTGAGGACGAAACATACTGAGAGTGTAGAGTGTGATGCTCCTGAGAATTCTGTTGTCTGGCAATCTTCAGCGGATGATGATAAGGTTGACGTGGTTTCGGGTTCTAGAAGATATGGATCTGAGAACTGGATGTCCTCAGCCAGGCATGAACCTACTTACACAGATTTGCTCTCCGGCTTTGGGACTAACATAGATCCATCCCATGGTCAGCGGATACCTTTTTATGACCATTCATCATCACCTTCTATGCCTGCAAAGAGAATCTTGAGTGATTCAGAAGGCAAGTTCGATTATCTTGCTAACCAGTGGCAGATGATACACTCTGGTCTCTCCCTGAAGTTACATGAATCTCCTAAGGTACCTGCAGCAACTGATGCGTCTCTCCAAGGGCGATGCAATGTTAAATACAGCGAATATCCTGTTCTTAATGGTCTATCGACTGAGAATGCTGGTGGTAACTGGCCAATACGTCCACGTGCTTTGAATTATTATGAGGAAGTGGTCAATGCTCAAGCGCAAGCTCAGGCTAGGGAGCAAGTAACAAAACAACCCTTCACGATACAAGAGGAGACAGCAAAGTCAAGAGAAGGGAACTGCAGGCTCTTTGGCATTCCTCTGACCAACAACATGAATGGGACAGACTCAACCATQTCTCAGAGAAACAACTTGAATGATGCTGCGGGGCTTACACAGATAGCATCACCAAAGGTTCAGGACCTTTCAGATCAGTCAAAAGGGTCAAAATCAACAAACGATCATCGTGAACAGGGAAGACCATTCCAGACTAATAATCCTCATCCGAAGGATGCTCAAACGAAAACCAACTCAAGTAGGAGTTGCACAAAGgtaaatttttgcaatatgtagcacaaagtgtatgaggttgtgataacccttgaatcacttttcaactaacacatgacacattgatgtaaagGTTCACAAGCAGGGAATTGCACTTGGCCGTTCAGTGGATCTTTCAAAGTTCCAAAACTATGAGGAGTTAGTCGCTGAGCTGGACAGGCTGTTTGAGTTCAATGGAGAGTTGATGGCTCCTAAGAAAGATTGGTTGATAGTTTACACAGATGAAGAGAATGATATGATGCTTGTTGGTGACGATCCTTGGCAgtaagattttgcaaattttccatcttagtttatatcgatgttagtgtttttcttataacactgacacaatgatctctcttgcagGGAGTTTTGTTGCATGGTTCGCAAAATCTTCATATACACGAAAGAGGAAGTGAGGAAGATGAACCCGGGGACTTTAAGCTGTAGGAGCGAGGAAGAAGCAGTTGTTGGGGAAGGATCAGATGCAAAGGACGCCAAGTCTGCATCAAATCCTTCATTGTCCAGCGCTGGGAACTCTTAAacaaacaaaataaccaacaacccttttgctgcaagccgaggtatgtaaaagcttttgagatattagtagactagagacacagccaaaagtttatgtcattacattcgactgatgtttgttctgttaatgacagcaggatgggggtcgattggtggagactggagagcaaaatgggatgatgggtttaagataagatattaaaaatgcaatttttgaagtattttgttggccacttagataattagcatcttccatcacccttattatctatctaataataattaatagatattataaagtaaaacataaaaaggttacaggtattatatagtagaatatgaaaagctcttttataagtagaatatgatggtgtggagttgtagtcggaggctggtatcggttctttttatggatgtatttttttccttcttccaaagatctcttgaagtctttttattgtttatattaatcccaatgtacataagttttcaagctcttgcccttttttaattatcttgtcgat tc SEQ ID NO. 2 MNTcomplete cDNA wild-type Col-0cccattggtcgcctcatacccagaaaaacaaaaggataggaaagacgaagaaataaaaagagagagaatgttagagagacaaactctgagagacaaaacaagagaaaatcgctcgtcgtcggtattcaagcgtctgtgactccgataaagcctagactagcgaggacggcgagagagagagagagagagctttggagttgtcgtatctctaaatcggaggcaatttgagtgagataaagacaaaggaaggaatcaagtggactaccgaagcgagttttgagctttttcagagacggatttggagatttcttgttgatatcgtctgcttagaggcttatttggtaccagatgaaacagatctgagcttcggaaggtatggcgagttcggaggtttcaatgaaaggtaatcgtggaggagataacttctcctcctctggttttagtgaccctaaggagactagaaatgtctccgtcgccggcgaggggcaaaaaagtaattctacccgatccgctgcggctgagcgtgctttggaccctgaggctgctctttacagagagctatggcacgcttgtgctggtccgcttgtgacggttcctagacaagacgaccgagtcttctattttcctcaaggacacatcgagcaggtggaggcttcgacgaaccaggcggcagaacaacagatgcctctctatgatcttccgtcaaagcttctctgtcgagttattaatgtagatttaaaggcagaggcagatacagatgaagtttatgcgcagattactcttcttcctgaggctaatcaagacgagaatgcaattgagaaagaagcgcctcttcctccacctccgaggttccaggtgcattcgttctgcaaaaccttgactgcatccgacacaagtacacatggtggattttctgttcttaggcgacatgcggatgaatgtctcccacctctggatatgtctcgacagcctcccactcaagagttagttgcaaaggatttgcatgcaaatgagtggcgattcagacatatattccggggtcaaccacggaggcatttgctacagagtgggtggagtgtgtttgttagctccaaaaggctagttgcaggcgatgcgtttatatttctaaggggcgagaatggagaattaagagttggtgtaaggcgtgcgatgcgacaacaaggaaacgtgccgtcttctgttatatctagccatagcatgcatcttggagtactggccaccgcatggcatgccatttcaacagggactatgtttacagtctactacaaacccaggacgagcccatctgagtttattgttccgttcgatcagtatatggagtctgttaagaataactactctattggcatgagattcaaaatgagatttgaaggcgaagaggctcctgagcagaggtttactggcacaatcgttgggattgaagagtctgatcctactaggtggccaaaatcaaagtggagatccctcaaggtgagatgggatgagacttctagtattcctcgacctgatagagtatctccgtggaaagtagagccagctcttgctcctcctgctttgagtcctgttccaatgcctaggcctaagaggcccagatcaaatatagcaccacatctcctgactcttcgatgcttaccagagaaggtacaactaaggcaaacatggaccctttaccagcaagcggactttcaagggtcttgcaaggtcaagaatactcgaccttgaggacgaaacatactgagagtgtagagtgtgatgctcctgagaattctgttgtctggcaatcttcagcggatgatgataaggttgacgtggtttcgggttctagaagatatggatctgagaactggatgtcctcagccaggcatgaacctacttacacagatttgctctccggctttgggactaacatagatccatcccatggtcagcggatacctttttatgaccattcatcatcaccttctatgcctgcaaagagaatcttgagtgattcagaaggcaagttcgattatcttgctaaccagtggcagatgatacactctggtctctccctgaagttacatgaatctcctaaggtacctgcagcaactgatgcgtctctccaagggcgatgcaatgttaaatacagcgaatatcctgttcttaatggtctatcgactgagaatgctggtggtaactggccaatacgtccacgtgctttgaattattatgaggaagtggtcaatgctcaagcgcaagctcaggctagggagcaagtaacaaaacaacccttcacgatacaagaggagacagcaaagtcaagagaagggaactgcaggctctttggcattcctctgaccaacaacatgaatgggacagactcaaccatgtctcagagaaacaacttgaatgatgctgcggggcttacacagatagcatcaccaaaggttcaggacctttcagatcagtcaaaagggtcaaaatcaacaaacgatcatcgtgaacagggaagaccattccagactaataatcctcatccgaaggatgctcaaacgaaaaccaactcaagtaggagttgcacaaaggttcacaagcagggaattgcacttggccgttcagtggatctttcaaagttccaaaactatgaggagttagtcgctgagctggacaggctgtttgagttcaatggagagttgatggctcctaagaaagattggttgatagtttacacagatgaagagaatgatatgatgcttgttggtgacgatccttggcaggagttttgttgcatggttcgcaaaatcttcatatacacgaaagaggaagtgaggaagatgaacccggggactttaagctgtaggagcgaggaagaagcagttgttggggaaggatcagatgcaaaggacgccaagtctgcatcaaatccttcattgtccagcgctgggaactcttaaacaaacaaaataaccaacaacccttttgctgcaagccgaggatgggggtcgattggtggagactggagagcaaaatgggatgatgggtttaagataagatattaaaaatgcaatttttgaagtattttgttggccacttagataattagcatcttccatcacccttattatctatctaataataattaatagatattataaagtaaaacataaaaaggttacaggtattatatagtagaatatgaaaagctcttttataagtagaatatgatggtgtggagttgtagtcggaggctggtatcggttctttttatggatgtatttttttccttcttccaaagatctcttgaagtctttttattgtttatattaatcccaatgtacataagttttcaagctcttgcccttttttaattatcttgtcgattc SEQ ID NO. 3 MNT predicted proteinwild-type Col-0 MASSEVSMKGNRGGDNFSSSGFSDPKETRNVSVAGEGQKSNSTRSAAAERALDPEAALYRELWHACAGPLVTVPRQDDRVFYFPQGHIEQVEASTNQAAEQQMPLYDLPSKLLCRVLNVDLKAEADTDEVYAQITLLPEANQDENAIEKEAPLPPPPRFQVHSFCKTLTASDTSTHGGFSVLRRHADECLPPLDMSRQPPTQELVAKDLHANEWRFRHIFRGQPRRHLLQSGWSVFVSSKRLVAGDAFIFLRGENGELRVGVRRAMRQQGNVPSSYISSHSMHLGVLATAWHAISTGTMFTVYYKPRTSPSEFIVPFDQYMESVKNNYSIGMRFKMRFEGEEAPEQRFTGTIVGIEESDPTRWPKSKWRSLKVRWDETSSIPRPDRVSPWKVEPALAPPALSPVPMPRPKRPRSNIAPSSPDSSMLTREGTTKANMDPLPASGLSRVLQGQEYSTLRTKHTESVECDAPENSVVWQSSADDDKVDVVSGSRRYGSENWMSSARHEPTYTDLLSGFGTNIDPSHGQRIPFYDHSSSPSMPAKRILSDSEGKFDYLANQWQMIHISGLSLKLIIESPKVPAATDASLQGRCNVKYSEYPVLNGLSTENAGGNWPIRPRALNYYEEVVNAQAQAQAREQVTKQPFTIQEETAKSREGNCRLFGIPLTNNMNGTDSTMSQRNNLNDAAGLTQIASPKVQDLSDQSKGSKSTNDHREQGRPFQTNNPHPKDAQTKTNSSRSCTKVHKQGIALGRSVDLSKFQNYEELVAELDRLFEFNGELMAPKKDWLIVYTDEENDMMLVGDDPWQEFCCMVRKIFIYTKEEVRKMNPGTLSCRSEEEAVVGEGSDAKDAKSA SNPSLSSAGNS SEQ IDNO. 4 mnt-1 genomic DNA Col-3AGCCATTTTGTAACTGACCACCGAGTAATCTGTAATCTGAGCTCTTTTATTAATCGGATTGAATAAATTCGCTTGGAGTCCGTCAGTCGTGTCCGTGAGCGCGTGTCTCACTCGCTTGAGCTGATGAAGTGCGATAATGACGTGGCATGTTGGGATGGAGACCAAAGACCAGCATTTTATTTTATTTTATAGTAACTAATTTTAAAAACCAAACAACCTGAGATTAAAATTTTAATTTTTACTGTACTGTAGTAAATTTGGGTCCTGATTAAGATTAGGCATATTTATCTCATAGTTTATAACAAGTAGCAGCTGAAATTTGTATTACTAGCTTATAGTAATTAAACTAAAAACTACGTTCCAGGTTTTAAATTATTGTTTAAAGAAGATATAATAATATATTAAGAAAATAGTTAATTAAGGTAAGGAGGAAAGTAGGGTTTGGTCTGTAGGTTAGGGTTCAAAGAGGGAAGAGATTAGGAGAAAGGAAGCATGAAGGCATGACCCATTTCTTCAATTAGTGCTCCTTAATCTGGTGACACGTGTAGGTCCCACGTGTAATCACTTCACATTGTTATTTTTCAAAAAATCAATTAGTAAAAACAAAACTTTGTCCATCATCAAATAGTAGTAGTTTTTTATGTGTGGTTACAATATTGTAAGAAGCTCTCCCCCTTTTACTATGTAATTCAACCCCACTCTAATTTTTAAAATATTTATGTAAAGCTTTACCCGAAAACAATCTATCATGGGTTGGTAATGACACATTTCATTAACAGTGTTAGAGAATGATTCCTTTAATTTTTCTACAGTAAAATGTTAGGTGATCTCATTGTACTACATCGGAAAATACTCAAAATTATGTCGTGTAATTTAGATAATGGACGAATATGGTTTTGAAATATTTATGGATACCCAACAAGATTTCTTAACTAGAAAGACAAAAAAATAGAGCACATTTTGCTCGTTTTCCATCAACCCTATTTCTCCAATTTGTTCACATCATGATCAAAAATACAGTAGCAATTAAAAAATAAAATAACAAATATAAATGGCTATATAGATCAACCCTATCTAGCTATTAGTATTACTAGAAATTGACAATAAAGGAAACATTCACGTGTGTGAGCATGTACTACTCTACACACATGTCCACAGTTATTATATACTGAGTACTAGTATACGTTGATGTTATCAATAATAAAAACTCGAAATTAAGTATTATTTTCTTATAATAATCTATTTAACCATATTTGCTACTGTACTATTTAGTCTATTTTCTTTTGCCAACCTTTGTATTAAATATTTGTACTATTAGTTTCAATTATAGGTCTATCACTATGTATATGTCCGAATAATGGTCTAAAATTGTTAATATAAAATACAGATTTTATTTCAGCTAAAGATAGTTGAAATTACACAAGAAAATAGAAGAGATAAAAATGATCAATCAGCTATGTAAGACGTCGTATGGATAGTTCAATAATTGTGGTAATACTTAAAGACATATATCAAAATTATCAACAAGCCTCGAACACAAACTTTACAAAAAGCCTGTGTCTACTTTATGAGTGTTTGATTATTAAATTGCAAGGTCGTAGTATAAAAATTTCGTAGGCTTTCAGGACACAAGATTAAATTCATTTATCTAAATGGTGATGGAGTACTTTTATTTTTATATATCAAAATGGTGATGATATACGAAGACCATATATTTAGATTATTAAAGAAAAAACGAGAAAAGAAGAAAGAAAATATAAAAAAATGGTTTTTCTTTTTAACGGACAAAGATTCCTACAATGGTTGCTTTTAGACCACACACAAATGCTACACAGTACTCTTGGGTCCCACACCTCTTAGCAAGTGCGTTACCAACACGTGAATTTCCTCTCCCCATTTTCTCGTCCTTTTCCTCTCAATATTGTATCGTCTCGTTTTCCTTGTCATATCGCGTGTGACGTGTTATTGGCTTATTGCTGAACAGTCTTCTTTTTTATTTTCCATCGTTATCCTGATTTTTTTTTTTTTCCAAATTTGATTTTCATGGTTTGTAATTTTGCAATAGATTTTGTGTTTCACAGAGAGATAGTTTACGTGTTGTTAAAAATAATTTGTGCAAAATAGTGTGCGTGTGTTAAATATTAAACGATATATAATAATTAGAAGAAAATAAAAAGTTTTGTCGCGATTAGTTATTTGATATTTACCTTGTTCTTTTGTTTATCGCTGCGACAAGCACCGACGGTATAAAATATAAAGAAAAAAAGAAAGAGAGATGAAGGTGAGATGAATGAAAGAGTCGCAGCGACAGATCTGAAGAGATAGGAGAAAGGGAATTTGAGACGCTGAAAATTCCAGCGTCTACGGAATGGCCGAATTACAGTCGATGCGGCAGAGATGAAAAAAATGAGAAATGAAAGTGAAAAAGAGATGAGAACTTTTTTTGGGTCGCAGGTAGCTGACGCAGCAATCAACAAAAGAACATGGCCAACGTTTTAGTAGATACTACTATAAAAGAAAAAGGTTGATTTAATTCATTCGTAATTTGGACTTAATTTTTTTTTAGGAACACTAATTAATCTTATTTGCCAGCTGTATGAGTGGACTACAATAAACTCTTGTCTATAAACCAGATTTTCTTCCTTTTTAACGCTTCCACTTACAACAATATATGTAAATATGTAATTATGACGGGGCATACGGAAATTTAATTTTTGAAGCAGATTCATCCCATTAGCCAGCTGTATTAAGTGGTAATCCAAGAGTTAATTTAGTTGTTCAGCAAATGATTTTAGATAAAATCAACTACTAGTTTAAAATAACTATCGAATGACTGTTAAGGCTTCGTATTTTTTGTTCTGCCATCAGGATATCATAAATATGGTTGAGGTTCGTATAATATTCGACGATCTTTTATATATCTGAGTTGTAATTGAATTAGAGAAAATAAAAAACAGATAATGAAACGTCTTTGTTTTTCCATAAAAAGAAAAACAGGGTAAATTAAAGTACGAGAGATTCACGAGACGAAAATTCCTAGAGGCGCACGATAGCCAAAAGACCATAGAAAATGACATCCGAAATATCTTTAAAATGCTAAAATGCACATATTTTTCTGGTGCCACGTAGCATTTTTCTCCCTCTCTCGTTCTCTCTACGTCCACCCAGACCTGCCTGTTCACAGCACGACAAAGCCACTTCCCAATAAAAACACAACACCTTTCCCATTGACGCTCTCTTTCCCAAACACCGTTATCCTCTTTACCCAATCAAAAGTTGACGCTTGCTCACGACTTGTTGACGCCGTTAGTCCCATCTAAAAAAGTAAAGCAGCCTTTCTTACTTGCTAATCCCCTCTACACATTTAATTTATTTTCTCCCCTAATGGATTTTTTTTGGCAACTTGAGTATTTATTTTTCAACTCACAGTAACTGTAAATAAATAAAAGTATTCAACTCACAGTCACCAGTAAATAAATACTACCAGACCATAGTTTTTTCAAGAATTGTTTTGGTCAACAATTTTAGGATGACTTAAATTGCTATATTTCTGGGGAAATACGACTTGGAAATGTCTGCAATTTGGGTCTTTTCTTCAATTTATCTTCTCCAATTTGTTTTTTAAAAAATTAAATTTTAGAAAAGGATATGTCAATTTTTTCTATTGAAAAGGCTTTATTAAAAAATAAGAAAAAGTGGAGGAAAGAAAATAAAATCGTCACTTGTCTTTGGTTTTGTGAGGTCGCAGACCCTGGTCCCCCGGAAATGGTTACAACCGGTAATAGCCGGTATGAAAGAGGGAATGGTAACCGGTGAATGCCGGTTATCCATATGGGTTAGAAGTTTACCGCGGTTGAAATGATTGAAGCTGAGTTTTGACTACCTCTGGTTAAGCCCATTGGTCGCCTCATACCCAGAAAAACAAAAGGATAGGAAAGACGAAGAAATAAAAAGAGAGAGAATGTTAGAGAGACAAACTCTGAGAGACAAAACAAGAGAAAATCGCTCGTCGTCGGTATTCAAGCGTCTGTGACTCCGATAAAGCCTAGACTAGCGAGGACGGCGAGAGAGAGAGAGAGAGAGCTTTGGAGTTGTCGTATCTCTAAATCGGAGGCAATTTGAGGTGAAATTGGTGGTTTTATCGTTTGATTCTAGGGTTTATCTTCTCTGATAGTTTTATCGAGTAATGTCAAGGAGCTAAACTAGTGGTGATTGTGTTTGTTAGTGAGATAAAGACAAAGGAAGGAATCAAGTGGACTACCGAAGCGAGTTTTGAGCTTTTTCAGAGACGGATTTGGAGATTTCTTGTTGATATCGTCTGCTTAGAGGCTTATTTGGTACCAGATGAAACAGATCTGAGCTTCGGAAGGTATGGCGAGTTCGGAGGTTTCAATGAAAGGTAATCGTGGAGGAGATAACTTCTCCTCCTCTGGTTTTAGTGACCCTAAGGAGACTAGAAATGTCTCCGTCGCCGGCGAGGGGCAAAAAAGTAATTCTACCCGATCCGCTGCGGCTGAGCGTGCTTGTAAGTCTCCGTTTCTTAGGGTTTCTTAAGCTTGGTTTTGGTTACAGACTGACTTGATCTAATTTATCTTCTTCTTCTTCGTCTTCATAGTGGACCCTGAGGCTGCTCTTTACAGAGAGCTATGGCACGCTTGTGCTGGTCCGCTTGTGACGGTTCCTAGACAAGACGACCGAGTCTTCTATTTTCCTCAAGGACACATCGAGCAGGTGAGATATTTCATCTATGAGTTCTTGCTATTTTTGGCTAAATCTTTGAGTTAACCCCTCTGTGATTCGTACCTGTTGAGATATTTTCTAATGAACTTTGTCGGTTTCCATTGTTTTATGATTAGGTGGAGGCTTCGACGAACCAGGCGGCAGAACAACAGATGCCTCTCTATGATCTTCCGTCAAAGCTTCTCTGTCGAGTTATTAATGTAGATTTAAAGGTAGGTTTCTTTAACTTCTTGGAAAATTTTGGTTTCTGTGTCTTGGATTGTCAGCTAACAAGAGTTTTGTTTATGATTTTACAAGCAGAGGCAGATACAGATGAAGTTTATGCGCAGATTACTCTTCTTCCTGAGGCTAATGTAAGTTTTGTTTTCTGATTTATTGGTTTGAGTGTTGTAGAGGTGATCTTATTCTTCAAGATGCTGAATTCTATATATTTTTTGTTCCATACAGCAAGACGAGAATGCAATTGAGAAAGAAGCGCCTCTTCCTCCACCTCCGAGGTTCCAGGTGCATTCGTTCTGCAAAACCTTGACTGCATCCGACACAAGTACACATGGTGGATTTTCTGTTCTTAGGCGACATGCGGATGAATGTCTCCCACCTCTGGTTGGTGTTTCATTTGCGCTTCTAACTATCTATTCATTGGCTTATTTTTCCTGAATTTTGTTCTAAGATTGCCTTCAATTCATTTTTTGTTTCTTCCCTCAGGATATGTCTCGACAGCCTCCCACTCAAGAGTTAGTTGCAAAGGATTTGCATGCAAATGAGTGGCGATTCAGACATATATTCCGGGGTATAGGAATCTGTAACTTTTTTATTTTCTGTTTTTCTCGAGTCTGTGTGTCATCAAACTTATCTGGTTGTTGATGTTTGTGATAATGGACCAGGTCAACCACGGAGGCATTTGCTACAGAGTGGGTGGAGTGTGTTTGTTAGCTCCAAAAGGCTAGTTGCAGGCGATGCGTTTATATTTCTAAGGTTTGTGGATTTTAGTTCATTGTTTTCTTTAGCTGTATCTGTTAGTTTCTATAATGTGGAATATCTTAATCTTCTACAGGGGCGAGAATGGAGAATTAAGAGTTGGTGTAAGGCGTGCGATGCGACAACAAGGAAACGTGCCGTCTTCTGTTATATCTAGCCATAGCATGCATCTTGGAGTACTGGCCACCGCATGGCATGCCATTTCAACAGGGACTATGTTTACAGTCTACTACAAACCCAGGTTTGTATTTGTATTAGCTCACAAAACAGCTTTCAGTTTTTTGAGCTCTTTGCTTTGTATGTCTCTATATGTCTGATGCTTGGTAGTGAATCACTCTACTAAATTTTCATGCGGTGTTGTTTTGTTTAATACAGGACGAGCCCATCTGAGTTTATTGTTCCGTTCGATCAGTATATGGAGTCTGTTAAGAATAACTACTCTATTGGCATGAGATTCAAAATGAGATTTGAAGGCGAAGAGGCTCCTGAGCAGAGGTAAAACCTGTCTTCTGCTTTTGAAATATGTTAGCTCTTGAGCCTTTTTCTCTTGGAATAACGAACCTAACAAGTTGTATTGATTTATATTAGGTTTACTGGCACAATCGTTGGGATTGAAGAGTCTGATCCTACTAGGTGGCCAAAATCAAAGTGGAGATCCCTCAAGGTATGACCTAGTTTCTAGAGAGGATCAAGACTATTGTTTGAATATAATGAATGCTGATTGTTCAATTGTCTTTCAGGTGAGATGGGATGAGACTTCTAGTATTCCTCGACCTGATAGAGTATCTCCGTGGAAAGTAGAGCCAGCTCTTGCTCCTCCTGCTTTGAGTCCTGTTCCAATGCCTAGGCCTAAGAGGCCCAGATCAAATATAGCACCTTCATCTCCTGACTCTTCGATGCTTACCAGAGAAGGTAATGTCTTCCCCTTCCACTGTAGTACACATAGTAGTGCGTCTGAAACTTAATTGAACTTGTCAGTGGGAGTCTAATTCATTGTACACAAAACAGGTACAACTAAGGCAAACATGGACCCTTTACCAGCAAGCGGACTTTCAAGGGTCTTGCAAGGTCAAGAATACTCGACCTTGAGGACGAAACATACTGAGAGTGTAGAGTGTGATGCTCCTGAGAATTCTGTTGTCTGGCAATCTTCAGCGGATGATGATAAGGTTGACGTGGTTTCGGGTTCTAGAAGATATGGATCTGAGAACTGGATGTCCTCAGCCAGGCATGAACCTACTTACACAGATTTGCTCTCCGGCTTTGGGACTAACATAGATCCATCCCATGGTCAGCGGATACCTTTTTATGACCATTCATCATCACCTTCTATGCCTGCAAAGAGAATCTTGAGTGATTCAGAAGGCAAGTTCGATTATCTTGCTAACCAGTGGCAGATGATACACTCTGGTCTCTCCCTGAAGTTACATGAATCTCCTAAGGTACCTGCAGCAACTGATGCGTCTCTCCAAGGGCGATGCAATGTTAAATACAGCGAATATCCTGTTCTTAATGGTCTATCGACTGAGAATGCTGGTGGTAACTGGCCAATACGTCCACGTGCTTTGAATTATTATGAGGAAGTGGTCAATGCTCAAGCGCAAGCTCAGGCTAGGGAGCAAGTAACAAAACAACCCTTCACGATACAAGAGGAGACAGCAAAGTCAAGAGAAGGGAACTGCAGGCTCTTTGGCATTCCTCTGACCAACAACATGAATGGGACAGACTCAACCATGTCTCAGAGAAACAACTTGAATGATGCTGCGGGGCTTACACAGATAGCATCACCAAAGGTTCAGGACCTTTCAGATCAGTCAAAAGGGTCAAAATCAACAAACGATCATCGTGAACAGGGAAGACCATTCCAGACTAATAATCCTCATCCGAAGGATGCTCAAACGAAAACCAACTCAAGTAGGAGTTGCACAAAGGTAAATTTTTGCAATATGTAGCACAAAGTGTATGAGGTTGTGATAACCCTTGAATCACTTTTCAACTAACACATGACACATTGATGTAAAGGTTCACAAGCAGGGAATTGCACTTGGCCGTTCAGTGGATCTTTCAAAGTTCCAAAACTATGAGGAGTTAGTCGCTGAGCTGGACAGGCTGTTTGAGTTCAATGGAGAGTTGATGGCTCCTAAGAAAGATTGGTTGATAGTTTACACAGATGAAGAGAATGATATGATGCTTGTTGGTGACGATCCTTGGCAGTAAGATTTTGCAAATTTTCCATCTTAGTTTATATCGATGTTAGTGTTTTTCTTATAACACTGACACAATGATCTCTCTTGCAGGGAGTTTTGTTGCATGGTTCGCAANATCTTCATATACACGAAAGAGGAAGTGAGGAAGATGAACCCGGGGACTTTAAGCTGTAGGAGCGAGGAAGAAGCAGTTGTTGGGGAAGGATCAGATGCAAAGGACGCCAAGTCTGCATCAAATCCTTCATTGTCCAGCGCTGGGAACTCTTAAACAAACAAAATAACCAACAACCCTTTTGCTGCAAGCCGAGGTATGTAAAAGCTTTTGAGATATTAGTAGACTAGAGACACAGCCAAAAGTTTATGTCATTACATTCGACTGATGTTTGTTCTGTTAATGACAGCAGGATGGGGGTCGATTGGTGGAGACTGGAGAGCAAAATGGGATGATGGGTTTAAGATAAGATATTAAAAATGCAATTTTTGAAGTATTTTGTTGGCCACTTAGATAATTAGCATCTTCCATCACCCTTATTATCTATCTAATAATAATTAATAGATATTATAAAGTAAAACATAAAAAGGTTACAGGTATTATATAGTAGAATATGAAAAGCTCTTTTATAAGTAGAATATGATGGTGTGGAGTTGTAGTCGGAGGCTGGTATCGGTTCTTTTTATGGATGTATTTTTTTCCTTCTTCCAAAGATCTCTTGAAGTCTTTTTATTGTTTATATTAATCCCAATGTACATAAGTTTTCAAGCTCTTGCCCTTTTT TAATTATCTTGTCGATTCSEQ ID NO. 5 mnt-1 cDNA translational start to stopATGGCGAGTTCGGAGGTTTCAATGAAAGGTAATCGTGGAGGAGATAACTTCTCCTCCTCTGGTTTTAGTGACCCTAAGGAGACTAGAAATGTCTCCGTCGCCGGCGAGGGGCAAAAAAGTAATTCTACCCGATCCGCTGCGGCTGAGCGTGCTTTGGACCCTGAGGCTGCTCTTTACAGAGNGCTATGGCACGCTTGTGCTGGTCCGCTTGTGACGGTTCCTAGACAAGACGACCGAGTCTTCTATTTTCCTCAAGGACACATCGAGCAGGTGGAGGCTTCGACGAACCAGGCGGCAGAACAACAGATGCCTCTCTATGATCTTCCGTCAAAGCTTCTCTGTCGAGTTATTAATGTAGATTTAAAGAGGCAGATACAGATGAAGTTTATGCGCAGATTACTCTTCTTCCTGAGGCTAATCAAGACGAGAATGCAATTGAGAAAGAAGCGCCTCTTCCTCCACCTCCGAGGTTCCAGGTGCATTCGTTCTGCAAAACCTTGACTGCATCCGACACAAGTACACATGGTGGATTTTCTGTTCTTAGGCGACATGCGGATGAATGTCTCCCACCTCTGGATATGTCTCGACAGCCTCCCACTCAAGAGTTAGTTGCAAAGGATTTGCATGCAAATGAGTGGCGATTCAGACATATATTCCGGGGTCAACCACGGAGGCATTTGCTACAGAGTGGGTGGAGTGTGTTTGTTAGCTCCAAAAGGCTAGTTGCAGGCGATGCGTTTATATTTCTAAGGGGCGAGAATGGAGAATTAAGAGTTGGTGTAAGGCGTGCGATGCGACAACAAGGAAACGTGCCGTCTTCTGTTATATCTAGCCATAGCATGCATCTTGGAGTACTGGCCACCGCATGGCATGCCATTTCAACAGGGACTATGTTTACAGTCTACTACAAACCCAGGACGAGCCCATCTGAGTTTATTGTTCCGTTCGATCAGTATATGGAGTCTGTTAAGAATAACTACTCTATTGGCATGAGATTCAAAATGAGATTTGAAGGCGAAGAGGCTCCTGAGCAGAGGTTTACTGGCACAATCGTTGGGATTGAAGAGTCTGATCCTACTAGGTGGCCAAAATCAAAGTGGAGATCCCTCAAGGTGAGATGGGATGAGACTTCTAGTATTCCTCGACCTGATAGAGTATCTCCGTGGAAAGTAGAGCCAGCTCTTGCTCCTCCTGCTTTGAGTCCTGTTCCAATGCCTAGGCCTAAGAGGCCCAGATCAAATATAGCACCTTCATCTCCTGACTCTTCGATGCTTACCAGAGAAGGTACAACTAAGGCAAACATGGACCCTTTACCAGCAAGCGGACTTTCAAGGGTCTTGCAAGGTCAAGAATACTCGACCTTGAGGACGAAACATACTGAGAGTGTAGAGTGTGATGCTCCTGAGAATTCTGTTGTCTGGCAATCTTCAGCGGATGATGATAAGGTTGACGTGGTTTCGGGTTCTAGAAGATATGGATCTGAGAACTGGATGTCCTCAGCCAGGCATGAACCTACTTACACAGATTTGCTCTCCGGCTTTGGGACTAACATAGATCCATCCCATGGTCAGCGGATACCTTTTTATGACCATTCATCATCACCTTCTATGCCTGCAAAGAGAATCTTGAGTGATTCAGAAGGCAAGTTCGATTATCTTGCTAACCAGTGGCAGATGATACACTCTGGTCTCTCCCTGAAGTTACATGAATCTCCTAAGGTACCTGCAGCAACTGATGCGTCTCTCCAAGGGCGATGCAATGTTAAATACAGCGAATATCCTGTTCTTAATGGTCTATCGACTGAGAATGCTGGTGGTAACTGGCCAATACGTCCACGTGCTTTGAATTATTATGAGGAAGTGGTCAATGCTCAAGCGCAAGCTCAGGCTAGGGAGCAAGTAACAAAACAACCCTTCACGATACAAGAGGAGACAGCAAAGTCAAGAGAAGGGAACTGCAGGCTCTTTGGCATTCCTCTGACCAACAACATGAATGGGACAGACTCAACCATGTCTCAGAGAAACAACTTGAATGATGCTGCGGGGCTTACACAGATAGCATCACCAAAGGTTCAGGACCTTTCAGATCAGTCAAAAGGGTCAAAATCAACAAACGATCATCGTGAACAGGGAAGACCATTCCAGACTAATAATCCTCATCCGAAGGATGCTCAAACGAAAACCAACTCAAGTAGGAGTTGCACAAAGGTTCACAAGCAGGGAATTGCACTTGGCCGTTCAGTGGATCTTTCAAAGTTCCAAAACTATGAGGAGTTAGTCGCTGAGCTGGACAGGCTGTTTGAGTTCAATGGAGAGTTGATGGCTCCTAAGAAAGATTGGTTGATAGTTTACACAGATGAAGAGAATGATATGATGCTTGTTGGTGACGATCCTTGGCAGGAGTTTTGTTGCATGGTTCGCAAAATCTTCATATACACGAAAGAGGAAGTGAGGAAGATGAACCCGGGGACTTTAAGCTGTAGGAGCGAGGAAGAAGCAGTTGTTGGGGAAGGATCAGATGCAAAGGACGCCAAGTCTGCATCAAATCCTTCATTGTCCAGCGCTGGGAACTCTTAA SEQ ID NO. 6 mnt-1 predicted protein Col-3MASSEVSMKGNRGGDNFSSSGFSDPKETRNVSVAGEGQKSNSTRSAAAERALDPEAALYRELWHACAGPLVTVPRQDDRVFYFPQGHIEQVEASTNQAAEQQMPLYDLPSKLLCRVINVDLKRQIQMKFMRRLLFFLRLIKTRMQLRKKR LFLHLRGSRCIRSAKP SEQID NO. 7 Forward primer for amplifying Brassica napus ARF2 5′ATGGCGAGTTCGGAGGTTT 3′ SEQ ID NO. 8 Reverse primer for amplifyingBrassica napus ARF2 5′ TGGACAATGAAGGATTTGATG 3′ SEQ ID NO. 9 BnARF2cDNA, translational start to stopATGGCGAGTTCGGAGGTTTCTATGAAAGGAAATCGTGGACGAGGAGAAAACTTCTCCTCCGCTGGTTACAGTGACCCGACGGTCGCCGGCGAGGCGCAGAAAACTCAGTCTAACCGATCTGTGGCTGCAGAGCGCGTTGTCGACCCGGAAGCTGCTCTCTACCGTGAGCTGTGGCACGCTTGTGCTGGTCCTCTCGTGACAGTCCCTCGACAAGATGACCGAGTCTTCTACTTCCCTCAGGGCACATCGAGCAGGTGGAAGCATCGACAAATCAAGCTGCAGAACAGCAGATGCCTCTCTATGATCTTCCTTCGAAGATCCTTTGTCGTGTCATTAATGTTGATTTAAAGGCAGAGGCAGACACCGACGAAGTTTATGCGCAGATTACTCTTCTTCCGGAGCCTGTTCAAGACGAGAATTCAATAGAGAAAGAGGCGCCTCCTCCTCCGCCCCCAAGGTTCCAAGTGCACTCCTTCTGCAAAACCTTGACTGCATCGGACACAAGTACACATGGTGGATTTTCTGTGCTTAGGCGGCATGCGGATGAATGTCTCCCACCTCTGGATATGTCACGTCAACCTCCTACTCAGGAGTTAGTTGCAAAAGATCTGCATGCAAGCGAGTGGCGTTTCCGACATATTTTCCGAGGTCAACCACGAAGGCATTTGCTTCAGAGTGGATGGAGCGTGTTTGTTAGCTCCAAGAGGCTGGTCGCAGGCGATGCTTTTATATTTCTAAGGGGCGAGAATGGAGAATTACGTGTGGGTGTAAGGCGTGCAATGCGGCAGCAAGGAAATGTGCCATCCTCTGTTATATCAAGCCACAGCATGCATCTCGGAGTATTGGCCACTGCCTGGCACGCTATTTCAACTGGAACCATGTTTACAGTCTACTATAAACCGAGGACTAGTCCTTCAGAGTTTATTGTTCCGTTTGATCAGTATACGGAGTCCGTGAAGATTAACTACTCCATAGGCATGAGATTTAAAATGAGATTTGAAGGCGAAGAGGCTCCCGAGCAGAGGTTTACTGGCACAATCGTTGGGATTGAAGACTCTGACCCCACGAGGTGGGCAAAATCAAAATGGAGATCCCTCAAGGTACGGTGGGATGAGACCACTAGTATTCCTCGCCCTGATAGAGTATCCCCGTGGAAGATAGAGCCAGCTCTTTCTCCTCCTGCTTTGAGCCCTGTACCAATGCCTAGGCCTAAGAGGCCCAGATCTAATCTAGCTTCTTCAACTCCGGACTCTTCCATGCGCATAAGGGAAGGCTCATCTAAGGCAAACATGGACCCTTTACCGGCAAGTGGACTATCAAGGGTCTTGCAAGGTCAAGAATACCCGACCTTGAGAACGAAACATGTTGAGAGTGTAGAATGCGATGCTCCTGAAAATTCGGTTGTGTGGCAATCGTCAACTGATGATGACAAGGTTGATGTGATTTCAGCTTCTAGGAGATATGAGAACTGGATATCCTCAGGTAGGCATGGACCTACTTGCACGGATTTGCTTTCTGGCTTTGGGACAAACATAGAACCACCTCACGGTCATCAGATACCTTTTTATGACCGTTTATCATCACCACCTTCTGTGGCTGCAAGGAAAATCCTCAGCGACCAGGATGGCAAGTTTGAATATCTTGCTAACCAGTGGATGATGCACTCAGGCCTTTCCCTGAAGTTACATGAATCTCCTAAAGTCCCTGCCGCATCTGATGCCTCTTTCCAAGGGATAGGCAATCCCAATTACGGCGAATATGCTTTGCCTCGTGCAGTGACGACTGAGAATGCTGCTGGCAACTGGCCAATACGTCCACGTGCTCTAAATTATTTTGAAGAAGCGGTTCATGCTCAGGCTAGAGAGCATGTGACAAAACGTCCTGCGGTCGTACAAGAGGAGGCAGCAAAGCCAAGAGACGGGAACTGCAGGCTTTTTGGCATTCCTCTGGTGAACAACGTGAATGGGACAGATACAACTTTGTCTCAGAGAAACAATTTGAATGACCCTGCGGGGCCTACGCAGATGGCATCACCAAAGGTTCAGGATCTTTCTGACCAGTCCAAAGGGTCAAAATCGACAAATGATCATCGTGAGCAAGGACGACCATTCCCGGTTAGTAAACCCCATCCGAAAGACGTTCAAACCAAAACAAACTCATGTAGGAGCTGCACGAAGGTTCAGAAGCAGGGGATTGCACTTGGCCGGTCAGTGGATCTCTCAAAGTTCCAGAACTATGAGGAGTTGGTTACTGAATTGGATAGGCTGTTTGAGTTCAATGGAGAGTTGATGGCTCCTAAGAAAGATTGGCTGATAGTTTACACAGATGATGAGAATGATATGATGCTTGTTGGAGACGATCCTTGGCAGGAGTTTTGTTGCATGGTTCGTAAAATCTTCATATACACGAAAGAGGAGGTCAGGAAGATGAACCCGGGAACTCTATGCTGTAGGAACGAGGAAGAACCAGTTGTTGGGGAAGGATCAGATGCAAAGGACGCGAAGTCTGCATCAAATCCTTCATTGTCCAGCGCCGGAAACTCTTAA SEQ ID NO. 10 BnARF2predicted protein MASSEVSMKGNRGRGENFSSAGYSDPTVAGEAQKTQSNRSVAAERVVDPEAALYRELWHACAGPLVTVPRQDDRVFYFPQGHIEQVEASTNQAAEQQMPLYDLPSKILCRVINVDLKAEADTDEVYAQITLLPEPVQDENSIEKEAPPPPPPRFQVHSFCKTLTASDTSTHGGFSVLRRHADECLPPLDMSRQPPTQELVARDLHASEWRFRHIFRGQPRRHLLQSGWSVIFVSSKRLVAGDAFIFLRGENGELRVGVRRAMRQQGNVPSSVISSHSMHLGVLATAWHAISTGTMFTVYYKPRTSPSEFIVPFDQYTESVKINYSIGMRFKMRFEGEEAPEQRFTGTIVGIEDSDPTRWAKSKWRSLKVRWDETTSIPRPDRVSPWKIEPALSPPALSPVPMPRPKRPRSNLASSTPDSSMRIREGSSKANMDPLPASGLSRVLQGQEYPTLRTKHVESVECDAPENSVVWQSSTDDDKVDVISASRRYIENWISSGRHGPTCTDLLSGFGTNIEPPHGHQIPFYDRLSSPPSVAARKILSDQDGKFEYLANQWMMHSGLSLKLHESPKVPAASDASFQGIGNPNYGEYALPRAVTTENAAGNWPIRPRALNYFEEAVHAQAREHVTKRPAVVQEEAAKPRDGNCRLFGIPLVNNVNGTDTTLSQRNNLNDPAGPTQMASPKVQDLSDQSKGSKLSTNDHREQGRPFPVSKPHPKDVQTKTNSCRSCTKVQKQGIALGRSVDLSKEQNYEELVTELDRLFEFNGELMAPKKDWLIVYTDDENDMMLVGDDPWQEFCCMVRKIFIYTKFEVRKMNPGTLCCRNEEEPVVGEGSDAKDAKSASNPSLSSAGN S

REFERENCES

-   Adams, S., Vinkenoog, R., Spielman, M., Dickinson, H. G., and    Scott, R. J. (2000). Parental imprinting in Arabidopsis thaliana    requires DNA methylation. Development 127, 2493-2502.-   Alexander, H. M. and Wulff, R. D. (1985). Experimental ecological    genetics in Plantago X. The effects of maternal temperature on seed    and seedling characters in P. lanceolata. Journal of Ecology 73,    271-282.-   Austin, R. B. (1980). Physiological limitations to cereal yields and    ways of rescuing them by breeding. In Opportunities for increasing    crop yields (eds R. G. Hurd, P. V. Biscoe, and C. Dennis), pp. 3-20.    Pitman, London.-   Alonso, J. M. et al. (2003). Genome-wide insertional mutagenesis of    Arabidopsis thaliana. Science 301, 653-657.-   Alonso-Blanco, C., Blankestijn-De Vries, H., Hanhart, C. J., and    Koornneef, M. (1999). Natural allelic variation at seed size loci in    relation to other life history traits of Arabidopsis thaliana PNAS    USA 96, 4710-4717.-   Baker, S. C., Robinson-Beers, K., Villanueva, J. M., Gaiser, J. C.,    and Gasser, C. S. (1997). Interactions among genes regulating ovule    developing in Arabidopsis thaliana. Genetics 145, 1109-24.-   Board, J. (2001). Reduced lodging for soybean in low plant    population is related to light quality. Crop Science 41, 379-384.-   Beeckman, T., De Rycke, R., Viane, R., and Inzé, D (2000).    Histological study of seed coat development in Arabidopsis thaliana.    Journal of Plant Research 113, 139-148.-   Bouman, F. (1975). Integument initiation and testa development in    some Cruciferae. Botanical Journal of the Linnean Society 70,    213-229.-   Bouman, F. (1984). The ovule. In Embryology of angiosperms    (ed. B. M. Johri), pp. 123-157. Springer, Berlin.-   Branen, J. K., Shintani, D. K., and Engeseth, N.J. (2003).    Expression of antisense acyl carrier protein-4 reduces lipid content    in Arabidopsis leaf tissue. Plant Physiology 132, 748-756.-   Brown, J. W. S. and Simpson, C. G. (1998). Splice site selection in    plant pre-mRNA splicing. Annual Review of Plant Physiology and Plant    Molecular Biology 49, 77-95.-   Chandrasekharan, M. B., Bishop, K. J., and Hall, T. C. (2003).    Module-specific regulation of the β-phaseolin promoter during    embryogenesis. Plant Journal 33, 853-866.-   Cheng, W.-H., Taliercio, E. W., and Chourey, P. S. (1996). The    Miniature1 seed locus of maize encodes a cell wall invertase    required for normal development of endosperm and maternal cells in    the pedicel. Plant Cell 8, 971-983.-   Choi, D. S., Lee, Y., Cho, H. T., and Kende, H. (2003). Regulation    of expansion gene expression affects growth and development in    transgenic rice plants. Plant Cell 15, 1386-1398.-   Clough, S. J. and Bent, A. F. (1998). Floral dip: a simplified    method for Agrobacterium-mediated transformation of Arabidopsis    thaliana. Plant Journal 16, 735-743.-   Debeaujon, I., Peeters, A. J. M., Léon-Kloosterziel, K. M., and    Koornneef, M. (2001). The TRANSPARENT TESTA12 gene of Arabidopsis    encodes a multidrug secondary transporter-like protein required for    flavonoid sequestration in vacuoles of the seed coat endothelium.    Plant Cell 13, 853-871.-   Devic, M., Guilleminot, J., Debeaujon, I., Bechtold, N., Bensaude,    E., Koornneef, M., Pelletier, G., and Delseny, M. (1999). The    BANYULS gene encodes a DFR-like protein and is a marker of early    seed coat development. Plant Journal 19, 387-398.-   Doyholos, M. K., and Sieburth, L. E. (2000). Separable    whorl-specific expression and negative regulation by enhancer    elements within the AGAMOUS second intron. Plant Cell 12, 1799-1810.-   Duvick, D. N. (1992) Genetic contributions to advances in yield of    United States maize. Maydica 37, 69-79.-   Esau (1965) Plant Anatomy (2^(nd) Edition) Wiyley N.Y.-   Ferreira, P. C. G., Hemerly, A. S., de Almeida Engler, J., Van    Montagu, M., Engler, G., and Inzé, D. (1994). Developmental    expression of the Arabidopsis cyclin gene cyc1At. Plant Cell 6,    1763-1774.-   Garcia, D., Saingery, V., Chambrier, P., Mayer, U., Jüirgens, G.,    and Berger, F. (2003). Arabidopsis haiku mutants reveal new controls    of seed size by endosperm. Plant Physiology 131, 1661-1670.-   Garcia, D., Fitz Gerald, J. N., and Berger, F. (2005). Maternal    control of integument cell elongation and zygotic control of    endosperm growth are coordinated to determine seed size in    Arabidopsis. Plant Cell 17, 52-60.-   Gleave, A. P. (1992). A versatile binary vector system with a T-DNA    organisational structure conducive to efficient integration of    cloned DNA into the plant genome. Plant Molecular Biology 20,    1203-1207.-   Goto, K. and Meyerowitz, E. M. (1994). Function and regulation of    the Arabidopsis floral homeotic gene PISTILLA TA. Genes and    Development 8, 1548-1560.-   Guberac, V., Martinic, J. and Maric, S. (1998). Influence of seed    size on germinability, germ length, root length and grain yield in    spring oat. Bodenkultur 49, 13-18.-   Hagen, G. and Guilfoyle, T. (2002). Auxin-responsive gene    expression: genes, promoters and regulatory factors. Plant Molecular    Biology 49, 373-385.-   Harper, J. L., Lovell, P. H., and Moore, K. G. (1970). The shapes    and sizes of seeds. Annual Review of Ecology and Systematics 1,    327-356.-   Hemerly, A., de Almeida Engler, J., Bergounioux, C., Van Montagu,    M., Engler, G., Inzé, D., and Ferreira, P. (1995). Dominant negative    mutants of the CDC2 kinase uncouple cell division from interative    plant development. EMBO Journal 14, 3925-3936.-   Hu, Y., Xie, Q., and Chua, N.-H. (2003). The Arabidopsis    auxin-inducible gene ARGOS controls lateral organ size. Plant Cell    15, 1951-1961.-   Jack, T., Brockman, L. L., and Meyerowitz, E. M. (1992). The    homeotic gene APETALA3 of Arabidopsis thaliana encodes a MADS box    and is expressed in petals and stamens. Cell 68, 683-697.-   Jefferson, R. A. (1987). Assaying chimeric genes in plants: the GUS    gene fusion system. Plant Molecular Biology Reporter 5, 387-405.-   Jofuku, K. D., Omidyar, P. K., Gee, Z., and Okamuro, J. K. (2005).    Control of seed mass and seed yield by the floral homeotic gene    APETALA2. PNAS 102, 3117-3122.-   Jones, R. J., Schreiber, B. M. N., and Roessler, J. A. (1996).    Kernel sink capacity in maize: genotypic and maternal regulation.    Crop Science 36, 301-306.-   Klucher, K. M., Chow, H., Reiser, L., and Fischer, R. L. (1996). The    AINTEGUMENTA gene of Arabidopsis required for ovule and female    gametophyte development is related to the floral homeotic gene    APETALA2. Plant Cell 8, 137-53.-   Krannitz, P. G., Aarssen, L. W., and Dow, J. M. (1991). The effect    of genetically based differences in seed size on seedling survival    in Arabidopsis thaliana (Brassicaceae). American Journal of Botany    78, 446-450.-   Leyser, O. (2002). Molecular genetics of auxin signaling. Annual    Review of Plant Biology 53, 377-398.-   Liscum, E. and Reed, J. W. (2002). Genetics of Aux/IAA and ARF    action in plant growth and development. Plant Molecular Biology 49,    387-400.-   Lopez-Dee, Z. P., Wittich, P., Pé, M. E., Rigola, D., del Buono, I.,    Sari Gorla, M., Kater, M. M., and Colombo, L. (1999). OsMADS13, a    novel rice MADS-box gene expressed during ovule development.    Developmental Genetics 25, 237-244.-   Mandel, A. M., Gustafson-Brown, C., Savidge, B., and Yanofsky, M. F.    (1992). Molecular characterization of the Arabidopsis floral    homeotic gene APETALA1. Nature 360, 273-277.-   Manga and Yadav (1995). Effect of seed size on developmental traits    and ability to tolerate drought in pearl-millet. Journal of Arid    Environments 29, 169-172.-   Marshall, D. L. (1986). Effect of seed size on seedling success in    three species of Sesbania (Fabaceae). American Journal of Botany 73,    457-464.-   Miliuviene, L., Novickiene, L., Gaveliene, V., Brazauskiene, I., and    Pakalniskyte, L. (2004). Possibilities to use growth regulators in    winter oilseed rape growing technology. 1. The effect of retardant    analogues on oilseed rape growth. Agronomy Research 2, 207-215.-   Moloney, M. M., Walker, J. M., and Sharma, K. K. (1989) Plant Cell    Reports 8, 238-242.-   Nahm, M. Y., Kim, S. W., Yun, D. J., Lee, S. Y., Cho, M. J., and    Bahk, J. D. (2003). Molecular and biochemical analysis of OsRAB7, a    rice Rab7 homolog. Plant and Cell Physiology 44, 1341-1349.-   Nesi, N., Debeaujon, I., Jond, C., Pelletier, G., Caboche, M., and    Lepiniec, L. (2000). The TT8 gene encodes a basic helix-loop-helix    domain protein required for expression of DFR and BAN genes in    Arabidopsis siliques. Plant Cell 12, 1863-1878.-   Nesi, N., Jond, C., Debeaujon, I., Caboche, M., and Lepiniec, L.    (2001). The Arabidopsis TT2 gene encodes an R2R3 MYB domain protein    that acts as a key determinant for proanthocyanidin accumulation in    developing seed. Plant Cell 13, 2099-2114.-   Nesi, N., Debeaujon, I., Jond, C., Stewart, A. J., Jenkins, G. I.,    Caboche, M., and Lepiniec. L. (2002). The TRANSPARENT TESTA16 locus    encodes the ARABIDOPSIS BSISTER MADS domain protein and is required    for proper development and pigmentation of the seed coat. Plant Cell    14, 2463-2479.-   Nicholas, K. B. and Nicholas, H. B., Jr. (1997). GeneDoc: a tool for    editing and annotating multiple sequence alignments.    http://www.psc.edu/biomed/genedoc-   Ohto, M., Fischer, R. L., Goldberg, R. B., Nakamura, K., and    Harada, J. J. (2005). Control of seed mass by APETALA2. PNAS 102,    3123-3128.-   Patrick, J. W. and Offler, C. E. (1995). Poist-sieve element    transport of sucrose in developing seeds. Australian Journal of    Plant Physiology 22, 681-702.-   Paul, M. J. and Foyer, C. H. (2001). Sink regulation of    photosynthesis. Journal of Experimental Botany 52, 1383-1400.-   Resier, L., Modrusan, Z., Margossian, L., Samach, A., Ohad, N.,    Haughn, G. W., and Fischer, R. L. (1995). The BELL1 gene encodes a    homeodomain protein involved in patter formation in the Arabidopsis    ovule primordium. Cell 83, 735-742.-   Reynolds, M. P., Skovmand, B., Trethowan, R. M., Singh, R. P., and    van Ginkel, M. (2001) Applying physiological strategies to wheat    breeding. Research highlights of the CIMMYT wheat program 1999-2000,    http://www.cimmyt.cgiar.org-   Robinson-Beers, K., Pruitt, R. E., and Gasser, C. S. (1992). Ovule    development in wild-type Arabidopsis and two female-sterile mutants.    Plant Cell 4, 1237-1249.-   Sagasser, M., Lu, G.-H., Hahlbrock, K., and Weisshaar, B. (2002). A.    thaliana TRANSPARENT TESTA 1 is involved in seed coat development    and defines the WIP subfamily of plant zinc finger proteins. Genes    and Development 16, 138-149.-   Sato, Y., Nishimura, A., Ito, M., Ashikari, M., Hirano, H.-Y., and    Matsuoka, M. (2001). Auxin response factor family in rice. Genes    Genet. Syst. 76, 373-380.-   Schaal, B A. (1980). Reproductive capacity and seed size in Lupinus    texensis. American Journal of Botany 67, 703-709.-   Schneitz, K., Hüilskamp, M., and Pruitt, R. E. (1995). Wild-type    ovule development in Arabidopsis thaliana: a light microscope study    of cleared whole-mount tissue. Plant Journal 7, 731-749.-   Scott, R. J, Spielman, M., Bailey, J., and Dickinson, H. G. (1998)    Parent-of-origin effects on seed development in Arabidopsis    thaliana. Development 125, 3329-3341.-   Soni, R., Carmichael, J. P., Shah, Z. H., and Murray, J. A. H.    (1995). A family of cyclin D homologs from plants differentially    controlled by growth regulators and containing the conserved    retinoblastoma protein interaction motif. Plant Cell 7, 85-103.-   Stals, H. and Inzé, D. (2001). When plant cells decide to divide.    Trends in Plant Science 6, 359-364.

Swank, J. C., Egli, D. B., and Pfeiffer, T. W. (1987). Seed growthcharacteristics of soybean genotypes differing in duration of seed fill.Crop Science 1, 85-89.

-   Takei, K., Sakakibara, H., and Sugiyama, T. (2001). Identification    of genes encoding adenylate isopentenyltransferase, a cytokinin    biosynthesis enzyme, in Arabidopsis thaliana. Journal of Biological    Chemistry 276, 26405-26410.-   Till, B. J. et al. (2003). Large-scale discovery of induced point    mutations with high-throughput TILLING. Genome Research 13, 524-530.-   Tiwari, S. B., Hagen, G., and Guilfoyle, T. J. (2003). The roles of    auxin response factor domains in auxin-responsive transcription.    Plant Cell 15, 533-543.-   Ulmasov, T., Hagen, G., and Guilfoyle, T. J. (1999a). Dimerization    and DNA binding of auxin response factors. Plant Journal 19,    309-319.-   Ulmasov, T., Hagen, G., and Guilfoyle, T. J. (1999b). Activation and    repression of transcription by auxin-response factors. PNAS USA 96,    5844-5849.-   Vandepoele, K., Raes, J., De Veylder, L., Rouze, P., Rombauts, S.,    and Inzé, D. (2002). Genome-wide analysis of core cell cycle genes    in Arabidopsis. Plant Cell 14, 1-16.-   Villanueva, J. M., Broadhvest, J., Hauser, B. A., Meister, R. J.,    Schneitz, K., and Gasser, C. S. (1999). INNER NO OUTER regulates    abaxial-adaxial patterning in Arabidopsis ovules. Genes and    Development 13, 3160-3169.-   Vinkenoog, R., Spielman, M., Adams, S., Fischer, R. L., and    Dickinson, H. G. (2000). Hypomethylation promotes autonomous    endosperm development and rescues post-fertilization lethality in    fie mutants. Plant Cell 12, 2271-2282.-   Wan, L., Xia, Q., Qui, X., and Selvaraj, G. (2002). Early stages of    seed development in Brassica napus: a seed coat-specific cysteine    proteinase associated with programmed cell death of the inner    integument. Plant Journal 30, 1-10.-   Wang, M.-B. and Waterhouse, P. M. (2001). Application of gene    silencing in plants. Current Opinion in Plant Biology 5, 146-150.-   Weber, H., Borisjuk, L., and Wobus, U. (1996). Controlling seed    development and seed size in Vicia faba: a role for seed    coat-associated invertases and carbohydrate state. Plant Journal 10,    823-824.-   Weber, H., Borisjuk, Ljudmilla, and Wobus, U. (1997). Sugar import    and metabolism during seed development. Trends in Plant Science 2,    169-174.-   Weigel, D., Alvarez, J., Smyth, D. R., Yanofksy, M. F., and    Meyerowitz, E. M. (1992). LEAFY controls floral meristem identity in    Arabidopsis. Cell 69, 843-859.-   Weschke, W., Panitz, R., Gubatz, S., Wang, Q., Radchuk, R., Weber,    H., and Wobus, U. (2003). The role of invertases and hexose    transporters in controlling sugar ratios in maternal and filial    tissues of barley caryopses during early development. Plant Journal    33, 395-411.-   Winn, A. A. (1985). Effects of seed size and microsite on seedling    emergence of Prunella vulgaris in four habitats. Journal of Ecology    73, 831-840.-   Wulff, R. D. (1986). Seed size variation in Desmondium    paniculatum II. Effects on seedling growth and physiological    performance. Journal of Ecology 74, 99-114.-   Yamada, T., Ito, M., and Kato, M. (2003). Expression pattern of    INNER NO OUTER homologue in Nymphaea (water lily family,    Nymphaeaceae). Development Genes and Evolution 213, 510-513.-   Zuber, U. Winzeler, H., Messmer, M. M., Keller, M., Keller, B.,    Schmid, J. E., and Stamp, P. (1999). Morphological traits associated    with lodging resistance of spring wheat (Triticum aestivum L.).    Journal of Agronomy and Crop Science 182, 17-24.

1. A method of modifying cell proliferation in a plant which comprisesmodulating the expression of a gene whose expression or transcriptionproduct is capable of directly or indirectly modulating cellproliferation in the plant or plant propagating material.
 2. A method ofmodifying cell proliferation in a plant which comprises the step oftransforming a plant, or plant propagating material, with a nucleic acidmolecule comprising at least one regulatory sequence capable ofdirecting expression within the integuments and/or seed coat of at leastone nucleic acid sequence whose expression or transcription product iscapable of directly or indirectly modulating cell proliferation.
 3. Amethod according to claim 1 or 2 in which the overall size of theinteguments/seed coat is modified.
 4. A method according to claim 1 or 2in which the function of a gene or gene product that promotes celldivision is enhanced or the function of a gene or gene product thatrepresses cell division is inhibited.
 5. A method according to claim 4in which cell division in the integuments/seed coat is increasedresulting in a larger seed of the plant compared to wild type. 6-9.(canceled)
 10. A method according to claim 5 in which the seed is atleast 5% heavier than wild type 11-19. (canceled)
 20. A method accordingto claim 1 or 2 in which the diameter of the stem of the plant is atleast 10% greater than wild type.
 21. (canceled)
 22. A method accordingto claim 1 or 2 in which the number of cells in the integuments/seedcoat is increased compared to wild type.
 23. (canceled)
 24. (canceled)25. A method according to claim 1 or 2 in which the sepal length of theplant is sufficiently greater than wild type to inhibit flower opening.26. A method according to claim 25 in which the sepal length is at least20% greater than wild type.
 27. (canceled)
 28. A method according toclaim 1 or 2 in which the function of a gene or gene product thatpromotes cell division is inhibited or the function of a gene productthat represses cell division is enhanced.
 29. A method according toclaim 28 in which cell division in the integuments/seed coat isdecreased resulting in a smaller seed compared to wild type.
 30. Amethod according to claim 29 in which the seed is at least 15% smallerthan wild type.
 31. A method according to claim 28 in which the numberof cells in the integuments/seed cost is decreased compared to wildtype.
 32. (canceled)
 33. (canceled)
 34. A method according to claim 1 or2 in which growth or development or function of any part of the plantother than the seed is not substantially affected.
 35. A methodaccording to claim 2 in which the regulatory sequence includes apromoter.
 36. A method according to claim 35 in which the promoter is aconstitutive promoter.
 37. A method according to claim 36 in which thepromoter directs gene expression in most or all cells of the plant. 38.A method according to claim 36 in which the promoter is the 35Spromoter.
 39. A method according to claim 35 in which the promoter isspecific, directing expression exclusively or primarily in one organ,tissue, or cell type of the plant.
 40. A method according to claim 39 inwhich the promoter directs expression exclusively or primarily in theinteguments or seed coat.
 41. A method according to claim 40 in whichthe promoter is expressed in the pre-fertilization integuments.
 42. Amethod according to claim 41 in which the promoter is the promoter ofthe INO or BEL1 gene.
 43. A method according to claim 42 in which thepromoter is expressed in the seed coat after fertilization.
 44. A methodaccording to claim 43 in which the promoter is the promoter of the BAN,TT1, TT2, TT8, TT12, or TT16 gene.
 45. A method according to claim 2 inwhich the nucleic acid sequence includes or is derived from a geneinvolved in hormone response, biosynthesis, translocation, or otheraspects of hormone action.
 46. A method according to claim 45 in whichthe gene is MNT, IPT1, or ARGOS or their orthologues.
 47. A methodaccording to claim 2 in which the nucleic acid sequence includes or isderived from a core cell cycle gene.
 48. A method according to claim 47in which the core cell cycle gene is CYCD3;1 or CYCB1;1 or theirorthologues.
 49. A method according to claim 2 in which the nucleic acidis a transcription factor involved in regulation of the extent or rateof cell proliferation.
 50. A method according to claim 49 in which thetranscription factor is ANT or its orthologue.
 51. A method according toclaim 3 in which the function of a gene that modulates cellproliferation is enhanced.
 52. A method according to claim 51 in whichtranscription of the gene is activated.
 53. A method according to claim52 in which activation of transcription results in increased levels ofmRNA and/or protein encoded by the gene.
 54. A method according to anyclaim 53 in which levels of mRNA and/or protein encoded by the gene areincreased by 20% or more.
 55. A method according to claim 1 or 2 inwhich a plant promoter is operably linked to a coding region of the genein the sense orientation.
 56. A method according to claim 3 to 55 inwhich the function of the gene is modulated by operably linking a plantpromoter to a nucleic acid fragment from the gene to form a recombinantnucleic acid molecule such that an antisense strand of RNA will betranscribed.
 57. A method according to claim 56, in which the functionof a gene is modulated by introducing nucleic acid segments of the geneinto an appropriate vector such that double-stranded RNA is transcribedwhere directed by an operably linked plant promoter.
 58. A methodaccording to claim 56 in which decreased levels of mRNA and/or proteinencoded by endogenous copies of the gene are produced.
 59. A methodaccording to claim 58 in which levels of mRNA and/or protein encoded byendogenous copies of the gene are decreased by 20%, 50% or 75% or more.60. A method according to claim 56 in which the levels of mRNA and/orprotein encoded by homologues of the gene are reduced.
 61. A methodaccording to claim 60 in which levels of mRNA and or protein encoded byhomologues of the gene are reduced by 20%, 50% or 75% or more.
 62. Amethod according to claim 2 in which the function of the gene ismodulated by operably linking a plant promoter to a ‘dominant negative’allele of the gene, which interferes with the function of the geneproduct.
 63. A method according to claim 2 in which the nucleic acidsequence comprises or is derived either from wild-type MNT or a mutantform of mnt or its orthologues.
 64. A method according to claim 1 or 2in which the plant is further modified to maintain desirablecharacteristics in other parts of the plant which may have been lost ormodified after the modulation or transformation step.
 65. A methodaccording to claim 64 in which the desirable characteristic isfertility.
 66. A method according to claim 65 in which wild type MNTfunction (or function of an MNT orthologue) is restored to petals andstamens of a transformed plant or an mnt mutant plant such that seedshave a modified phenotype but fertility is not impaired.
 67. A methodaccording to claim 66 in which the promoter of a gene that directsexpression in petals and stamens but not carpels is operably linked tothe wild-type MNT gene or an MNT orthologue.
 68. A method according toclaim 67 in which the promoter is the promoter of the AP3 gene.
 69. Amethod according to claim 1 or 2 in which the plant is monocotyledonous.70. A method according to claim 69 in which the plant is a crop plant.71. (canceled)
 72. A method according to claim 1 or 2 in which the plantis dicotyledonous.
 73. (canceled)
 74. A method according to claim 1 or 2in which the plant is subsequently bred to be homozygous for themodulated gene.
 75. A method according to claim 2 in which plant is bredto be heterozygous for the modulated gene.
 76. A plant which comprises,within the integuments and/or seed coats of the plant, a modulated genewhose expression or transcription product is capable of directly orindirectly modulating cell proliferation in the plant or plantpropagating material.
 77. A plant which includes a nucleic acid moleculecomprising at least one regulatory sequence capable of directingexpression within the integuments and/or seed coat of at least onenucleic acid sequence whose expression or transcription product iscapable of directly or indirectly modulating cell proliferation.
 78. Aplant according to claim 76 or 77 in which the overall size of theinteguments/seed coat in the plant is modified.
 79. A plant according toclaim 76 or 77 in which the function of a gene or gene product thatpromotes cell division is enhanced or the function of a gene or geneproduct that represses cell division is inhibited.
 80. A plant accordingto claim 79 in which cell division in the integuments/seed coat isincreased resulting in a larger seed compared to wild type. 81-84.(canceled)
 85. A plant according to claim 80 to 84 in which the seed isat least 5% heavier than wild type. 86-94. (canceled)
 95. A plantaccording to claim 76 or 77 in which the diameter of the stem of themodified or transformed plant is at least 10% greater than wild type.96. (canceled)
 97. A plant according to claim 76 or 77 in which thesepal length of the plant is sufficiently greater than wild type toinhibit flower opening.
 98. A plant according to claim 97 in which thesepal length is at least 20% greater than wild type.
 99. (canceled) 100.A plant according to claim 76 or 77 in which the number of cells in theinteguments/seed coat of the plant is increased compared to wild type.101. (canceled)
 102. (canceled)
 103. A plant according to claim 76 or 77in which the function of a gene or gene product that promotes celldivision is inhibited or the function of a gene product that repressescell division is enhanced.
 104. A plant according to claim 103 in whichcell division in the integuments/seed coat is decreased resulting in asmaller seed compared to wild type.
 105. A plant according to claim 104in which the seed is at least 5% smaller than wild type. 106-108.(canceled)
 109. A plant according to claim 104 in which the seed is atleast 5% lighter than wild type. 110-112. (canceled)
 113. A plantaccording to claim 76 or 77 in which the number of cells in theinteguments/seed cost is decreased compared to wild type.
 114. A plantaccording to claim 113 in which the number of cells in theinteguments/seed coat is decreased by at least 30% compared to wildtype.
 115. A plant according to claim 76 or 77 in which growth ordevelopment of any part of the plant other than the seed is notsubstantially affected.
 116. A plant according to claim 76 in which theregulatory sequence includes a promoter.
 117. A plant according to claim116 in which the promoter is a constitutive promoter.
 118. A plantaccording to claim 117 in which the promoter directs gene expression inmost or all cells of the plant.
 119. A plant according to claim 117 inwhich the promoter is the 35S promoter.
 120. A plant according to claim116 in which the promoter is specific, directing expression exclusivelyor primarily in one organ, tissue, or cell type of the plant.
 121. Aplant according to claim 120 in which the promoter directs expressionexclusively or primarily in the integuments or seed coat.
 122. A plantaccording to claim 121 in which the promoter is expressed in thepre-fertilization integuments.
 123. A plant according to claim 122 inwhich the promoter is the promoter of the INO or BEL1 gene.
 124. A plantaccording to claim 120 in which the promoter is expressed in the seedcoat after fertilization.
 125. A plant according to claim 124 in whichthe promoter is the promoter of the BAN, TT1, TT2, TT8, TT12, or TT16gene.
 126. A plant according to claim 77 in which the nucleic acidsequence includes or is derived from a gene involved in hormoneresponse, biosynthesis, translocation, or other aspects of hormoneaction.
 127. A plant according to claim 126 in which the gene is MNT,IPT1, or ARGOS or their orthologues.
 128. A plant according to claim 77in which the nucleic acid sequence includes or is derived from a corecell cycle gene.
 129. A plant according to claim 128 in which the corecell cycle gene is CYCD3;1 or CYCB1;1 or their orthologues.
 130. A plantaccording to claim 77 in which the nucleic acid encodes a transcriptionfactor involved in regulation of the extent or rate of cellproliferation.
 131. A plant according to claim 130 in which thetranscription factor is ANT or its orthologue.
 132. A plant according toclaim 76 or 77 in which the function of a gene that modulates cellproliferation is enhanced.
 133. A plant according to claim 132 in whichtranscription of the gene is activated
 134. A plant according to claim133 in which activation of transcription results in increased levels ofmRNA and/or protein encoded by the gene.
 135. A plant according to claim134 in which levels of mRNA and/or protein encoded by the gene areincreased by at least 20%.
 136. A plant according to claim 76 or 77 inwhich a plant promoter is operably linked to a coding region of the genein the sense orientation.
 137. A plant according to claim 76 or 77 inwhich the function of the gene is modulated by introducing a nucleicacid segments of the gene into an appropriate vector such thatdouble-stranded RNA is transcribed where directed by an operably linkedplant promoter.
 138. A plant according to claim 137, in which thefunction of the gene is modulated by operably linking a plant promoterto a nucleic acid segment from the gene, and introducing the resultingrecombinant nucleic acid into an appropriate vector such thatdouble-stranded RNA is transcribed.
 139. A plant according to claim 137in which decreased levels of mRNA and/or protein encoded by endogenouscopies of the gene are produced.
 140. A plant according to claim 139 inwhich levels of mRNA and/or protein encoded by endogenous copies of thegene are reduced by at least 50%.
 141. A plant according to claim 137 inwhich the levels of mRNA and protein encoded by homologues of the geneare reduced.
 142. A plant according to claim 141 in which the levels ofmRNA and protein encoded by homologues of the gene are reduced by 50% ormore.
 143. A plant according to claim 76 or 77 in which the function ofthe gene is modulated by operably linking a plant promoter to a‘dominant negative’ allele of the gene, which interferes with thefunction of the gene product.
 144. A plant according to claim 76 or 77in which the modulated gene or nucleic acid sequence comprises or isderived either from wild-type MNT or a mutant form of mnt or itsorthologues.
 145. A plant according to claim 76 or 77 in which the plantis further modified to maintain desirable characteristics in other partsof the plant which may have been lost or modified.
 146. A plantaccording to claim 145 in which the desirable characteristic isfertility.
 147. A plant according to claim 146 in which wild type MNTfunction (or the function of an MNT orthologue) is restored to petalsand stamens of the plant or an mnt mutant plant such that seeds have amodified phenotype but so that fertility is not impaired.
 148. A plantaccording to claim 147 in which the promoter of a gene that directsexpression in petals and stamens but not carpels is operably linked to awild type MNT gene or an MNT orthologue.
 149. A plant according to claim148 in which the promoter is the promoter of the AP3 gene.
 150. A plantaccording to claim 76 or 77 in which the plant is monocotyledonous. 151.A plant according to claim 150 in which the plant is a crop plant. 152.(canceled)
 153. A plant according to claim 76 or 77 in which the plantis dicotyledonous.
 154. (canceled)
 155. A plant according to claim 77 inwhich the plant has been bred to be homozygous for the modified gene.156. A plant according to claim 77 which is heterozygous for themodified gene.
 157. A method for modifying cell proliferation in a plantwhich comprises the step of modulating the response of the plant to anauxin in which cell proliferation is modified to produce larger orsmaller seeds than wild-type.
 158. A method according to claim 157 inwhich the response to an auxin is modulated by altering the expressionof an auxin response factor.
 159. A method according to claim 158 inwhich the auxin response factor inhibits cell division.
 160. A methodaccording to claim 159 in which the auxin response factor inhibits celldivision in the integuments/seed coat.
 161. A method according to claim160 in which the auxin response factor is ARF2.
 162. A method accordingto claim 157 in which the function or expression of the auxin responsefactor is inhibited.
 163. A method according to claim 162 in which thefunction or expression of the auxiliary response factor is specificallyinhibited in the integument/seed coat of the plant.
 164. A methodaccording to claim 157 in which a gene encoding the auxin responsefactor is modified so as to affect expression of the factor.
 165. Amethod according to claim 164 in which the gene is MNT or an orthologuethereof.